JP2007306893A - Processed salt - Google Patents

Processed salt Download PDF

Info

Publication number
JP2007306893A
JP2007306893A JP2006141877A JP2006141877A JP2007306893A JP 2007306893 A JP2007306893 A JP 2007306893A JP 2006141877 A JP2006141877 A JP 2006141877A JP 2006141877 A JP2006141877 A JP 2006141877A JP 2007306893 A JP2007306893 A JP 2007306893A
Authority
JP
Japan
Prior art keywords
salt
bittern
magnesium
component
drying
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.)
Granted
Application number
JP2006141877A
Other languages
Japanese (ja)
Other versions
JP4652278B2 (en
Inventor
Yoshiaki Nagaoka
義明 長岡
Asao Nakayama
朝雄 中山
Akiyoshi Masamune
明桂 正宗
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.)
Ako Kasei Co Ltd
Original Assignee
Ako Kasei 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 Ako Kasei Co Ltd filed Critical Ako Kasei Co Ltd
Priority to JP2006141877A priority Critical patent/JP4652278B2/en
Publication of JP2007306893A publication Critical patent/JP2007306893A/en
Application granted granted Critical
Publication of JP4652278B2 publication Critical patent/JP4652278B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

<P>PROBLEM TO BE SOLVED: To obtain salt free from discoloring food even in using for food in a powdery condition while containing bittern component. <P>SOLUTION: The salt containing bittern component is obtained by drying and/or baking treating while suppressing production of alkaline component such as magnesium oxide. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、べとつきのないにがり塩に関する。
また、本発明は、食品を変色させることなく、さらさらして使いやすい、にがり成分を含む塩に関する。
さらに詳しくは、本発明は、にがり成分を含んだ塩を原料として、アルカリ成分の生成を抑制しつつ、乾燥及び/又は焼成処理した塩に関する。
The present invention relates to non-sticky bittern salt.
The present invention also relates to a salt containing a bittern component that is easy to use without being discolored.
More specifically, the present invention relates to a salt that has been dried and / or calcined while using a salt containing a bittern component as a raw material while suppressing the formation of an alkali component.

近年、栄養学の進歩にともない、ミネラル成分の重要性が注目を集めるようになった。海水に含まれるにがりには、マグネシウム、カルシウム、カリウム、鉄、亜鉛、マンガン等のミネラル成分が含まれて、特にマグネシウムの補給源として、にがりは重要な役割を果たしてきた。
にがり塩に含まれるミネラルをより多く摂取するために、例えば特開平11−42064号公報では、有機酸又は有機酸塩を1.0%以上添加することにより、2.5%以上の多量のにがりを含む塩の苦味を緩和して、風味のある塩を経済的に提供することが提案されている。
また、マグネシウム補給及び味改良のため、にがりを適度に含む塩が一般に認知されており、多種多数の商品が販売されている。しかし、にがりの主成分である塩化マグネシウムは水分との親和性が高く、いわゆるにがり塩はべたべたした状態のため、食品に付着させる用途では敬遠されている現状がある。
In recent years, with the advancement of nutrition, the importance of mineral components has attracted attention. The bittern contained in seawater contains mineral components such as magnesium, calcium, potassium, iron, zinc, and manganese, and bittern has played an important role as a supplemental source of magnesium.
In order to ingest more minerals contained in bittern salt, for example, in JP-A-11-42064, a large amount of bittern of 2.5% or more is added by adding 1.0% or more of an organic acid or an organic acid salt. It has been proposed to economically provide a savory salt by alleviating the bitter taste of the salt.
Moreover, a salt containing moderate bittern is generally recognized for magnesium supplementation and taste improvement, and a large number of products are sold. However, magnesium chloride, which is the main component of bittern, has a high affinity for moisture, and so-called bittern salt is sticky, so there is a current situation where it is avoided for use in foods.

このため、にがり塩のべとつきを改良するために、古くから焼塩が用いられてきた。塩を焼くことにより水分が蒸発すると共に、塩中に含有される塩化マグネシウムが塩基性塩化マグネシウム及び/又は酸化マグネシウム等に変わり、塩化マグネシウムの吸湿を抑えることで、さらっとした状態の塩に変わる。例えば、特開平3−257015号公報に記載されている焼塩の製造方法は,Mg塩の含有量が0.05%以上の塩を500〜700℃で焼成する。
この条件で焼成すると、塩に含有される塩化マグネシウムは,塩基性塩化マグネシウムを経て酸化マグネシウムに変わり、サラサラ性が改良されると記載されている。また、特開平7−142号公報では、立方体塩を400℃〜融点以下の温度で平衡になるまで加熱した後、急冷することで微細な網目状のクラックを持つ加工塩が提案されている。
For this reason, baked salt has long been used to improve the stickiness of bittern salt. Moisture evaporates by baking the salt, and the magnesium chloride contained in the salt is changed to basic magnesium chloride and / or magnesium oxide, etc., and the moisture absorption of the magnesium chloride is suppressed to change to a salt in a dry state. . For example, in the method for producing a baked salt described in JP-A-3-257015, a salt having an Mg salt content of 0.05% or more is baked at 500 to 700 ° C.
It is described that when calcined under this condition, magnesium chloride contained in the salt is converted to magnesium oxide through basic magnesium chloride, and the smoothness is improved. Japanese Patent Application Laid-Open No. 7-142 proposes a processed salt having fine mesh-like cracks by heating a cubic salt at a temperature of 400 ° C. to a melting point or lower until equilibrium is reached, and then rapidly cooling.

一方、にがり成分を焼成によって塩基性塩化マグネシウム及び/又は酸化マグネシウムに変化させた焼塩は、水分を含んだとき水酸化物イオンを生成することでアルカリ性を示し、米飯等の穀物加工品に付着させた際に、表面を変色させる。塩基性塩化マグネシウム及び/又は酸化マグネシウムが水と接触した際の反応は以下のものと考えられる。   On the other hand, baked salt in which bittern component is changed to basic magnesium chloride and / or magnesium oxide by baking shows alkalinity by generating hydroxide ions when it contains moisture, and it adheres to processed grain products such as cooked rice. The surface changes color. The reaction when basic magnesium chloride and / or magnesium oxide comes into contact with water is considered as follows.

Mg(OH)Cl → Mg2++OH+Cl
MgO+H2O →→ Mg2++2OH
Mg (OH) Cl → Mg 2+ + OH + Cl
MgO + H 2 O →→ Mg 2+ + 2OH

上記アルカリによる変色の対象は、フラボノイドと呼ばれる色素で、ほとんどすべての植物の組織に含まれている。酸性及び中性域で安定であるが、アルカリ性で環状構造が壊れることで黄色く発色する。   The target of discoloration due to alkali is a pigment called flavonoid, which is contained in almost all plant tissues. Although it is stable in the acidic and neutral range, it develops yellow when it is alkaline and the cyclic structure is broken.

特開平11−42064号公報JP-A-11-42064 特開平3−257015号公報JP-A-3-257015 特開平7−142号JP-A-7-142

本発明では、にがり成分を含んだ塩を、酸化マグネシウム等のアルカリ成分の生成を抑制しつつ、乾燥及び/又は焼成処理し、水分を含んだ食品に使用しても変色させないさらさらした塩を提供することを課題とする。   In the present invention, a salt containing a bittern component is dried and / or baked while suppressing the formation of an alkali component such as magnesium oxide, and a free-flowing salt that does not change color even when used in a food containing moisture is provided. The task is to do.

本発明者らは、にがり塩の乾燥及び/又は焼成処理の際に生成する酸化マグネシウム等のアルカリ成分量に着目し、前記課題を解決すべく鋭意研究した結果、含有するにがり成分の量と乾燥及び/又は焼成処理条件を規定することにより、水分を含んだ食品に使用しても変色しないことを見出し、本発明を完成するに至った。   The present inventors paid attention to the amount of alkali components such as magnesium oxide produced during the drying and / or baking treatment of bittern salt, and as a result of earnest research to solve the above problems, the amount of the bittern component contained and drying And / or by specifying baking process conditions, it discovered that even if it used for the foodstuff containing a water | moisture content, it discovered that it did not discolor and came to complete this invention.

本発明は、にがり成分と水分を含んだ塩を、酸化マグネシウム等のアルカリ成分の生成を抑制しつつ、乾燥及び/又は焼成処理したことを特徴とする塩に関するものである。原料となる塩混合物のマグネシウム量は0.10%〜4.0%である。0.10%未満では、にがりを含んだ塩というには不十分である。
一方、4.0%を越えると、苦味が強く、食品加工用途に適さず、好ましくは0.10%〜1.5%である。塩の乾燥及び/又は焼成処理は、0℃〜250℃の温度範囲で行なわれる。
この際のアルカリ成分の生成量を、酸化マグネシウム換算で0.0%〜0.1%に、好ましくは0.0%〜0.03%に制御する。処理後の塩が、さらさらになる水分量は0.0%〜1.0%であり、好ましくは0.0%〜0.3%である。
The present invention relates to a salt obtained by drying and / or firing a salt containing a bittern component and moisture while suppressing generation of an alkaline component such as magnesium oxide. The amount of magnesium in the salt mixture as a raw material is 0.10% to 4.0%. If it is less than 0.10%, it is not sufficient for a salt containing bittern.
On the other hand, if it exceeds 4.0%, the bitterness is strong and it is not suitable for food processing applications, preferably 0.10% to 1.5%. The salt is dried and / or calcined in a temperature range of 0 ° C to 250 ° C.
The production amount of the alkali component at this time is controlled to 0.0% to 0.1%, preferably 0.0% to 0.03% in terms of magnesium oxide. The water content of the salt after treatment is 0.0% to 1.0%, preferably 0.0% to 0.3%.

本発明により、にがり成分を含んでいるにも関わらず、さらさらとして使いやすく、水分の多い穀物加工品に振りかけても変色させることのない塩が得られた。したがって、にがりのミネラル成分を含み、味が良く、さらに使いやすい食品加工用の塩である。   According to the present invention, although a bittern component is contained, a salt that is easy to use more easily and does not change color even when sprinkled on a processed grain product with a high amount of water was obtained. Therefore, it is a salt for food processing that contains bittern mineral components, has a good taste and is easy to use.

本発明の原料となる塩は、天日塩、天日塩溶解後再晶析塩、イオン交換塩、岩塩、地下鹹水晶析塩、海洋深層水塩等が好ましいが、特に種類は選ばない。
原料の塩に含まれるにがり成分が少なければ、適量のにがりを添加し、混合してもよい。
栄養として有用な各種ミネラル補給の観点から、マグネシウムとして0.1%以上のにがりの添加量でなければならない。
食用塩の適正な商品表示を図るために、業界の主要企業が参加して食用塩公正競争規約作成準備会が平成16年9月に発足した。取りまとめられた食用塩公正競争規約〔案〕では、当該食用塩がにがりを含有し、かつマグネシウムの含有量が乾燥基準で0.1%以上の場合に限り、にがりと表示することができるとしており、このこともマグネシウム含量が0.1%以上でなければならないことを裏付けている。
一方、4.0%を超えるマグネシウムを含む塩は、にがりによる苦味が強すぎ食味を低下させる。そのうえ吸湿性が高いため、さらさらにするための乾燥及び/又は焼成条件が厳しくなり、アルカリ成分の生成を抑制しにくい。
原料となる塩又は製品の塩の粒径は特にこだわらない。使用する上で適当でなければ、粉砕機で細かくしてもよく、また造粒機で大粒にしてもよい。
塩ににがり以外の成分を加えて、製品に他の機能を付与してもよい。機能成分としては、固結防止剤、栄養強化剤、調味料、その他が挙げられる。これらの成分には、アルカリ性のものもあり、過剰な添加によって食品を黄変させないよう注意が必要である。一方、調味料の中の酸味料は酸性を示すため、にがり由来のアルカリ成分の、食品への作用を減弱する。添加量によっては、食品の黄変を防止する方法になりうるが、酸味が食品の味覚に影響しないよう注意が必要である。
The salt used as a raw material of the present invention is preferably sun salt, recrystallized salt after sun salt dissolution, ion exchange salt, rock salt, underground crystal crystallization salt, deep sea water salt, etc., but the type is not particularly selected.
If the bittern component contained in the salt of the raw material is small, an appropriate amount of bittern may be added and mixed.
From the viewpoint of supplementing various minerals useful as nutrition, the amount of bittern must be 0.1% or more as magnesium.
In September 2004, a preparation group for the preparation of fair competition rules for edible salt was established with the participation of major companies in the industry in order to display appropriate products for edible salt. The compiled edible salt fair competition rules [draft] states that garlic can be displayed only if the edible salt contains bittern and the magnesium content is 0.1% or more on a dry basis. This also confirms that the magnesium content must be 0.1% or more.
On the other hand, a salt containing magnesium exceeding 4.0% has a too bitter taste due to bittern and lowers the taste. In addition, since the hygroscopic property is high, the drying and / or firing conditions for further improvement become severe, and it is difficult to suppress the production of alkali components.
The particle size of the salt as the raw material or the salt of the product is not particularly limited. If it is not suitable for use, it may be fined with a pulverizer or may be made large with a granulator.
Components other than bittern may be added to the salt to impart other functions to the product. Examples of the functional component include an anti-caking agent, a nutrient enhancer, a seasoning, and others. Some of these components are alkaline, and care must be taken not to yellow the food by excessive addition. On the other hand, since the acidulant in the seasoning shows acidity, the action of the alkaline component derived from bittern on the food is attenuated. Depending on the amount added, it can be a method to prevent yellowing of food, but care must be taken so that the acidity does not affect the taste of the food.

水分を減少させてさらさらの塩にするために、乾燥及び/又は焼成処理を行なう。処理の設備としては、加熱及び/又は減圧が可能で混合や払出しのしやすい、陶製及び硝子製及びプラスチック製及び金属製容器、万能混合機、リボン式混合機、真空流動乾燥機、振動流動乾燥機、凍結乾燥機、リボコーン、ロータリーキルン、噴霧乾燥機、パルコン乾燥機、等が好ましいが、これらに限定されない。
このとき、塩中の塩化マグネシウムを高温にすると、塩基性塩化マグネシウム及び/又は酸化マグネシウム等のアルカリ成分が生成する。非常に高温で生成する酸化カルシウム、酸化カリウム等も原因物質になる。
A drying and / or baking process is performed in order to reduce moisture to a free salt. Processing facilities include ceramic, glass, plastic and metal containers, universal mixers, ribbon mixers, vacuum fluidized dryers, vibratory fluidized dryers that can be heated and / or decompressed and mixed and dispensed easily. A machine, a freeze dryer, a ribocorn, a rotary kiln, a spray dryer, a pulcon dryer, and the like are preferable, but not limited thereto.
At this time, when the magnesium chloride in the salt is heated to a high temperature, basic components such as basic magnesium chloride and / or magnesium oxide are generated. Calcium oxide, potassium oxide, etc. produced at very high temperatures are causative substances.

処理後の塩を中和滴定法で定量分析することで、酸化マグネシウムに換算したアルカリ成分量を測定することができる。アルカリ成分量が酸化マグネシウム換算で0.0%〜0.1%の塩であれば、水分豊富な穀類加工食品に使用しても変色が抑制されるが、さらに好ましくは0.0%〜0.03%である。処理後の塩は水分が減少してさらさらとなり、流動性が高く使いやすい性状となる。その際の水分量は0.0%〜1.0%であり、さらに好ましくは、0.0%〜0.3%である。   By quantitatively analyzing the salt after the treatment by a neutralization titration method, the amount of alkali component converted to magnesium oxide can be measured. If the amount of alkali component is 0.0% to 0.1% in terms of magnesium oxide, discoloration is suppressed even when used in processed foods rich in moisture, but more preferably 0.0% to 0 0.03%. The salt after the treatment has a reduced moisture content and becomes smooth, and has a high fluidity and is easy to use. The moisture content in that case is 0.0%-1.0%, More preferably, it is 0.0%-0.3%.

以下に本発明の実施例を詳細に説明するが、本発明はこの実施例に限定されるものではない。
塩田産天日塩を溶解、再晶析させる。得られた晶析塩を脱水して、水分量5%以下の塩を調製した。
この塩に、最終のマグネシウム濃度が約0.1%、0.3%、0.5%、0.7%、0.9%となるようににがりを混合し、にがり塩とした。にがり塩100gを蒸発皿に広げ、200℃に予備加熱した卓上型マッフル炉に設置し、温度一定で0.5時間加熱した。処理後は、すべてのサンプルがさらさらした性状の塩となった。
このときのアルカリ成分は、酸化マグネシウム換算で0.02〜0.15%となった。
Examples of the present invention will be described in detail below, but the present invention is not limited to these examples.
Dissolve and recrystallize the salt salt from Shioda. The obtained crystallized salt was dehydrated to prepare a salt having a water content of 5% or less.
To this salt, bittern was mixed so that the final magnesium concentration was about 0.1%, 0.3%, 0.5%, 0.7%, and 0.9% to obtain a bittern salt. 100 g of bittern salt was spread on an evaporating dish, placed in a desktop muffle furnace preheated to 200 ° C., and heated at a constant temperature for 0.5 hour. After treatment, all samples became free-flowing salt.
The alkali component at this time was 0.02 to 0.15% in terms of magnesium oxide.

マグネシウム含量は、キレート滴定法で求めた。
水分の測定は、塩を105℃定置乾燥機(品番:LC−112 TABAI ESPEC CORP製)で恒量になるまで乾燥し、残渣量を塩量で除し、この値に100を乗じて求めた。
処理後の塩を中和滴定法で分析し、酸化マグネシウム換算でのアルカリ成分量を求めた。
成型した米飯100gに、片面当たり0.4gの塩(1個分合計0.8g)をふりかけ、1.5時間及び5時間後に目視観察した。黄色い変色の指標として色差計(品番:TC−8600A 日本電色工業(株)製)のb*値を測定した。
サンプル塩の分析値、性状、米飯に振りかけた際の色の変化を表1にまとめ、酸化マグネシウム換算でのアルカリ成分量と米飯の黄変の関係を示した。
The magnesium content was determined by chelate titration method.
The moisture was measured by drying the salt with a 105 ° C. stationary drier (product number: LC-112, TABI ESPEC CORP) until it became a constant weight, dividing the amount of residue by the amount of salt, and multiplying this value by 100.
The salt after the treatment was analyzed by a neutralization titration method to determine the amount of alkali component in terms of magnesium oxide.
100 g of the cooked cooked rice was sprinkled with 0.4 g of salt per side (total 0.8 g per piece) and visually observed after 1.5 hours and 5 hours. The b * value of a color difference meter (product number: TC-8600A manufactured by Nippon Denshoku Industries Co., Ltd.) was measured as an index of yellow discoloration.
Table 1 summarizes the analysis values, properties, and changes in color when sprinkled on cooked rice, and shows the relationship between the amount of alkali components in terms of magnesium oxide and the yellowing of cooked rice.

Figure 2007306893
Figure 2007306893

(表1の評価)
上記表1中の塩1〜3は、にがりを含んでいながらさらさらした塩であるが、アルカリ成分の量が少なく、米飯を変色させなかった。
これに対して、塩4と塩5は、乾燥及び/又は焼成処理により多くのアルカリ成分が生成し、米飯の表面に付着した際に黄色く変色させた。
つまり酸化マグネシウム換算のアルカリ成分が、0.02%、0.05%、0.08%では米飯の色は変化せず、0.12%と0.15%では黄変した。
(Evaluation of Table 1)
Salts 1 to 3 in Table 1 above were free-flowing salts containing bittern, but the amount of the alkaline component was small and the cooked rice was not discolored.
On the other hand, when the salt 4 and the salt 5 produced many alkali components by the drying and / or baking treatment and adhered to the surface of the cooked rice, they were changed to yellow.
That is, when the alkali component in terms of magnesium oxide was 0.02%, 0.05%, and 0.08%, the color of the cooked rice did not change, and yellowing occurred at 0.12% and 0.15%.

最終のマグネシウム濃度が0.13%となるにがり塩130kgを万能混合攪拌機(品番:250XDMV―QRS (株)DALTON製)の釜に投入し、攪拌するとともに釜を110℃〜130℃に加熱する。釜内部には高圧のエアーを送り込み、常に強制換気する。開始から20分後、40分後、120分後のサンプルを採取し、同様の分析を行なった。
サンプル塩の分析値、性状、米飯に振りかけた際の色の変化を表2にまとめ、塩の水分量と性状の関係を示した。
The final magnesium concentration is 0.13%, and 130 kg of bittern salt is charged into a pot of a universal mixing stirrer (product number: 250XDMV-QRS, manufactured by DALTON), stirred, and heated to 110 ° C to 130 ° C. High-pressure air is sent into the kettle, and forced ventilation is always performed. Samples were collected 20 minutes, 40 minutes, and 120 minutes after the start, and the same analysis was performed.
The analytical values, properties, and color changes when sprinkled on cooked rice are summarized in Table 2, and the relationship between the moisture content of the salt and the properties is shown.

Figure 2007306893
Figure 2007306893

(表2の評価)
塩8は、乾燥・焼成が不十分のため、べとべとで使いにくい塩であるのに対して、塩6及び塩7は、適切な処理により、さらさらの性状でかつ米飯の表面に付着した際に黄色く変色しない塩となった。
つまり、塩の水分が0.16%と0.76%ではさらさらの性状だったが、1.21%ではべとべとになった。
(Evaluation of Table 2)
Salt 8 is a salty and difficult to use salt due to insufficient drying and baking, whereas salt 6 and salt 7 have a dry nature and adhere to the surface of cooked rice by appropriate treatment. The salt became yellow and did not change color.
In other words, when the salt moisture was 0.16% and 0.76%, it was smooth, but when it was 1.21%, it became sticky.

最終のマグネシウム濃度が5.0%、3.0%、1.5%、0.13%となるにがり塩100gを蒸発皿に広げ、卓上型マッフル炉に設置し、110℃で3時間加熱した。処理後は、すべてのサンプルがさらさらした性状の塩となった。
味の確認のため、財団法人塩事業センターの食塩を対照とし、これらのサンプルを用いて官能検査を行なった。社内パネラー8名を用い、苦味の強い方を1として順番に1〜5の順位をつけさせ(順位法)、Kramerの検定表により評価を行なった。
サンプル塩の分析値、性状、米飯に振りかけた際の色の変化と官能検査の結果を表3にまとめ、塩全体のマグネシウム濃度と食味の関係を示した。
表中の官能検査における順位合計値において、15以下と33以上との間に5%の危険率で有意差がある。
The final magnesium concentration is 5.0%, 3.0%, 1.5%, and 0.13%. 100 g of bittern salt is spread on an evaporating dish, placed in a desktop muffle furnace, and heated at 110 ° C. for 3 hours. . After treatment, all samples became free-flowing salt.
In order to confirm the taste, sensory tests were performed using these samples, using salt from the salt business center as a control. Eight in-house panelists were used, and the one with strong bitterness was assigned to 1 in order of 1 to 5 (ranking method), and the evaluation was performed according to Kramer's test table.
Table 3 summarizes the analysis values, properties, and sensory test results of the sample salt when sprinkled on cooked rice, and shows the relationship between the magnesium concentration of the whole salt and the taste.
There is a significant difference at a risk rate of 5% between 15 or less and 33 or more in the ranking total value in the sensory test in the table.

Figure 2007306893
Figure 2007306893

(表3の評価)
すべてさらさらして米飯を変色させない塩であるが、塩9は5%危険率で有意に苦く、官能的に好まれなかった。過剰に含まれたにがり成分が、強い苦味を感じさせた。
一方、塩10、11、12はにがりを含んだ塩であるが食味の低下がなく、さらさらの性状で、米飯の表面に付着した際に黄色く変色させない塩だった。
又、塩13はもともとにがりを含有しない塩であり、にがり塩としての有用性が存在しない。
つまり、マグネシウム濃度が4.9%の塩は苦く、3.1%、1.5%および0.13%の塩は問題ない食味であり、0.01%の食塩はにがり塩ではない。
(Evaluation of Table 3)
Although it is a salt that does not discolor the cooked rice by freezing all the time, salt 9 was significantly bitter at a 5% risk factor and was not sensuously preferred. The bittern component contained in excess caused a strong bitter taste.
On the other hand, the salts 10, 11, and 12 were salt containing bittern, but there was no deterioration in the taste, and the salt was smooth and did not turn yellow when attached to the surface of cooked rice.
The salt 13 is originally a salt that does not contain bittern, and has no utility as bittern salt.
That is, a salt with a magnesium concentration of 4.9% is bitter, and 3.1%, 1.5% and 0.13% of the salt have no problem, and 0.01% of salt is not a bitter salt.

最終のマグネシウム濃度が約0.3%となるにがり塩100gを蒸発皿に広げ、卓上型マッフル炉に設置し、約100℃、200℃、300℃で0.5時間加熱した。
同じ原料10gを凍結乾燥機(品番:FD−1 東京理科機械(株)製)に設置し、約−40℃での予備凍結後に、真空条件で48時間乾燥した。
サンプル塩の分析値、性状、米飯に振りかけた際の色の変化を表4にまとめ、乾燥・焼成条件と米飯の黄変との関係を示した。
The final magnesium concentration was about 0.3%, 100 g of bittern salt was spread on an evaporating dish, placed in a tabletop muffle furnace, and heated at about 100 ° C., 200 ° C., and 300 ° C. for 0.5 hour.
10 g of the same raw material was placed in a freeze dryer (product number: FD-1 manufactured by Tokyo Science Machine Co., Ltd.), and after preliminary freezing at about −40 ° C., it was dried under vacuum conditions for 48 hours.
The analytical values, properties, and color changes when sprinkled on the cooked rice are summarized in Table 4, and the relationship between the drying and baking conditions and the yellowing of the cooked rice is shown.

Figure 2007306893
Figure 2007306893

(表4の評価)
上記表4中の塩14は、塩を予備凍結後に減圧条件で乾燥させた、いわゆる凍結乾燥法によるサンプルであるが、さらさらで米飯を変色させない塩ができた。
塩15と塩16は、比較的低温の条件による乾燥及び/又は焼成で水分を減少させたため、アルカリ成分の生成が抑制され、米飯の表面に付着した際に黄色く変色させることがない。
塩17と塩18は、にがりを含んだ塩だが、高温による処理でさらさらにしており、生成するアルカリ成分によって米飯が黄変する。
つまり、0℃以下の条件の凍結乾燥法、100℃および200℃の条件の塩は米飯が黄変せず、300℃と500℃の条件の塩は米飯が黄変した。
(Evaluation of Table 4)
The salt 14 in Table 4 above was a sample by a so-called freeze-drying method in which the salt was dried under reduced pressure after preliminary freezing, but a salt that did not discolor the cooked rice was produced.
Since the salt 15 and the salt 16 were reduced in moisture by drying and / or firing under relatively low temperature conditions, the production of alkali components was suppressed, and the salt 15 and the salt 16 did not turn yellow when adhered to the surface of cooked rice.
Although salt 17 and salt 18 are salt containing bittern, they are further processed by treatment at high temperature, and the cooked rice is yellowed by the generated alkali component.
That is, the lyophilization method under the condition of 0 ° C. or less, the salt under the conditions of 100 ° C. and 200 ° C. did not yellow the cooked rice, and the salt under the conditions of 300 ° C. and 500 ° C. yellowed the cooked rice.

Claims (7)

にがり成分を含んだ塩を、アルカリ成分の生成を抑制しつつ、乾燥及び/又は焼成処理したことを特徴とする塩。   A salt obtained by drying and / or baking treatment of a salt containing a bittern component while suppressing generation of an alkali component. アルカリ成分の生成量が、酸化マグネシウム含量換算で0.0重量%(以降%と表記)〜0.1%であることを特徴とする請求項1に記載の塩。   2. The salt according to claim 1, wherein the production amount of the alkali component is 0.0% by weight (hereinafter referred to as “%”) to 0.1% in terms of magnesium oxide content. アルカリ成分が、塩基性塩化マグネシウム及び/又は酸化マグネシウムであることを特徴とする請求項1又は2に記載の塩。   The salt according to claim 1 or 2, wherein the alkali component is basic magnesium chloride and / or magnesium oxide. 塩中の水分含量が0.0%〜1.0%であることを特徴とする請求項1〜3のいずれかに記載の塩。   The salt according to any one of claims 1 to 3, wherein the water content in the salt is 0.0% to 1.0%. 塩中のマグネシウム含量が0.10%〜4.0%であることを特徴とする請求項1〜4のいずれかに記載の塩。   The salt according to any one of claims 1 to 4, wherein a magnesium content in the salt is 0.10% to 4.0%. 乾燥及び/又は焼成処理が、0℃〜250℃の温度範囲で行なわれることを特徴とする請求項1〜5のいずれかに記載の塩。   The salt according to any one of claims 1 to 5, wherein the drying and / or baking treatment is performed in a temperature range of 0 ° C to 250 ° C. 使用した食品の変色を防止することを特徴とする請求項1〜6のいずれかに記載の塩及びその塩を使用した食品。
Discoloration of the used food is prevented, The food using the salt and the salt according to any one of claims 1 to 6.
JP2006141877A 2006-05-22 2006-05-22 Processed salt Active JP4652278B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2006141877A JP4652278B2 (en) 2006-05-22 2006-05-22 Processed salt

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2006141877A JP4652278B2 (en) 2006-05-22 2006-05-22 Processed salt

Publications (2)

Publication Number Publication Date
JP2007306893A true JP2007306893A (en) 2007-11-29
JP4652278B2 JP4652278B2 (en) 2011-03-16

Family

ID=38840331

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006141877A Active JP4652278B2 (en) 2006-05-22 2006-05-22 Processed salt

Country Status (1)

Country Link
JP (1) JP4652278B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010138017A (en) * 2008-12-10 2010-06-24 Hakatako Kanri Kk Salt-parching apparatus

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03257015A (en) * 1990-03-07 1991-11-15 Sakito Seien Kk Production of roast salt
JPH06153854A (en) * 1992-11-19 1994-06-03 Japan Tobacco Inc Edible salt containing bittern
JPH06169721A (en) * 1992-12-10 1994-06-21 Japan Tobacco Inc Fine-powder edible salt and its production
JP2000229281A (en) * 1999-02-09 2000-08-22 Omron Corp Production of salt
JP2005312301A (en) * 2004-03-31 2005-11-10 Seiichiro Yamamoto Common salt composition

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03257015A (en) * 1990-03-07 1991-11-15 Sakito Seien Kk Production of roast salt
JPH06153854A (en) * 1992-11-19 1994-06-03 Japan Tobacco Inc Edible salt containing bittern
JPH06169721A (en) * 1992-12-10 1994-06-21 Japan Tobacco Inc Fine-powder edible salt and its production
JP2000229281A (en) * 1999-02-09 2000-08-22 Omron Corp Production of salt
JP2005312301A (en) * 2004-03-31 2005-11-10 Seiichiro Yamamoto Common salt composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010138017A (en) * 2008-12-10 2010-06-24 Hakatako Kanri Kk Salt-parching apparatus

Also Published As

Publication number Publication date
JP4652278B2 (en) 2011-03-16

Similar Documents

Publication Publication Date Title
US10752871B2 (en) Preparation of a powdered vinegar
CA2578163C (en) Method for reducing acrylamide formation in thermally processed foods
KR100745302B1 (en) Method for reducing acrylamide formation in thermally processed foods
DK2512989T3 (en) NON-CONSUMPTIONAL POTASSIUM CHLORIDE COMPOSITION, PROCEDURE FOR ITS PREPARATION AND APPLICATION
EP1150578A1 (en) Physiological food salt product
CN106858521B (en) Process for preparing low sodium salt
US10005670B2 (en) Calcium polyphosphate salt particles and method of making
JP4652278B2 (en) Processed salt
JP2008069136A (en) Hygienic treatment agent with quicklime as active ingredient, and sterilizing/bactericidal method using the same
CA2909315C (en) Food salt product
KR101969692B1 (en) 2 Iron Ferrous Sources
JP6952705B2 (en) Dehydrated NA2-IMP as anti-caking agent
JP5251019B2 (en) How to prevent caking of salts
DK2928322T3 (en) PROCEDURE FOR MANUFACTURING MINERAL SALTS AND MINERAL SALTS PRODUCT
DK158330B (en) PROCEDURE FOR TREATING CEREALS OR SEEDS, WHEREAS THE CORE OR SEEDS ARE CONTACTED WITH AN OILY BEAR
JP2004065016A (en) Mineral-containing solution, method for producing the solution, and product using the solution
WO2023037952A1 (en) Acetic-acid-containing powder
JP7281290B2 (en) Method for producing boiled Chinese noodles
JP2006141287A (en) Corn powder excellent in dispersibility and having good flavor and method for producing the same
JP6994752B2 (en) Method for manufacturing powder composition for noodle making
KR20170037575A (en) Manufacture method of calcium containing composition which has high solubility in water
KR101831415B1 (en) Natural seasoning composition comprising glutamic acid and sun-dried salt
JP2012090538A (en) Saltiness-imparting preparation, and food using the same
JP2002058449A (en) Method for producing young leaf powder
JPH08107770A (en) Salty seasoning

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20090202

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20100621

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20100713

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20100910

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20101019

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20101116

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20101207

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20101215

R150 Certificate of patent or registration of utility model

Ref document number: 4652278

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20131224

Year of fee payment: 3

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250