JP2011073149A - Reversible thermal recording material - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a reversible thermal recording material having high texture whiteness and image erasability, and having satisfactory image storability when stored under a high temperature and high humidity environment. <P>SOLUTION: This reversible thermal recording material includes a thermal recording layer containing a dye precursor colorless or light-colored usually, and a reversible color developer of generating a reversible tone change in the dye precursor by a difference in a cooling speed after heated, on at least one face of a support body, and the thermal recording layer contains the reversible color developer of specified structure and an erasure promoter of specified structure. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

  The present invention relates to a reversible thermosensitive recording material whose color tone reversibly changes with temperature.

  A reversible thermosensitive recording material whose color tone changes reversibly according to temperature is capable of repeating image recording / erasing a plurality of times. In addition to magnetic recording layers and non-contact IC chips, it is used for prepaid cards, point cards, commuter passes, coupon tickets, entrance / exit management cards, examination tickets, logistics tags, manufacturing process control tables, labels, etc. It is also used as a display material for digital paper and electronic bulletin boards.

  In a reversible thermosensitive recording material, a reversible thermosensitive recording layer containing a dye precursor and a reversible developer that causes a reversible color change in the dye precursor is provided on a support. Clear image contrast, high-density image recording, almost complete erasure, recorded images can be retained in daily life environments, and more than 100 times of image recording and erasing are possible As a reversible developer, a phenol compound has been proposed (for example, Patent Documents 1 to 3).

  Many of the phenolic compounds used as reversible developers have an aliphatic hydrocarbon group at the molecular end. Due to the presence of this aliphatic hydrocarbon group, the dye precursor and the reversible developer are low in compatibility, and in a solidified state, they hardly melt and become decolored. When heated and melted, the dye precursor and the reversible developer are melted together to form a colored state. When slowly cooled from this color development state, the dye precursor and the reversible developer are phase-separated, return to a state where they hardly dissolve, solidify, become decolored, and the image can be erased. On the other hand, when rapidly cooled from the colored state, the dye precursor and the reversible developer are solidified before phase separation, and the colored state can be maintained, and an image can be recorded.

  Further, reversible developers in which unsaturated bonds are introduced into a part of the aliphatic hydrocarbon group of the phenol compound have been proposed (for example, Patent Documents 2, 4, and 5). For example, an unsaturated bond introduced for the purpose of changing the properties of the reversible thermosensitive recording material can be polymerized by introducing an acrylic group or a methacryl group, and the reversible developer is polymerized by light or heat. An image forming material capable of irreversibly fixing a decolored state (for example, Patent Document 6), less unerased at the time of erasing, and reversible that can be erased uniformly at a lower temperature and in a wide temperature range. And heat sensitive recording materials (for example, Patent Documents 7 and 8).

  Further, by including a specific organic amine or urea compound as an erasing accelerator, further erasability is improved (for example, Patent Documents 9 and 10).

  The reversible thermosensitive recording material is actually used under a wide range of environmental conditions from low temperature and low humidity to high temperature and high humidity. The above-described reversible thermosensitive recording materials using the reversible developer have problems that color development and erasure are liable to occur at low temperatures and low humidity, and high-speed erasure is difficult, and satisfactory image recording / erasing characteristics are not always obtained. It wasn't.

JP-A-5-124360 JP-A-10-95175 Japanese Patent Laid-Open No. 7-179043 Japanese Patent Laid-Open No. 10-861 Japanese Patent Laid-Open No. 10-6655 JP 2000-85250 A JP 2001-180122 A JP 2009-29088 A JP-A-6-270544 JP-A-6-320862

  An object of the present invention is to provide a reversible thermosensitive recording material that is excellent in color developability and can cope with high-speed decoloring properties in a low-temperature and low-humidity environment.

  The present inventors have developed a reversible color developer and an erasure promoting agent that form a relatively colored state on the support, usually a colorless or light-colored dye precursor, depending on the heating temperature and / or the cooling rate after heating. In the reversible thermosensitive recording material containing an agent, the above-mentioned problems can be solved by using a specific phenol compound as the reversible developer and a specific compound as the erasure accelerator, respectively. It came to complete.

  That is, the present invention provides a reversible sensation in which a reversible thermosensitive recording layer comprising a dye precursor, a reversible developer that causes a reversible color change in the dye precursor, and an erasing accelerator is provided on a support. In the thermal recording material, the reversible developer is a compound represented by the general formula (1), and the erasure accelerator contains at least one compound represented by the general formula (2) or (3). The above problem has been solved by a reversible thermosensitive recording material characterized by the above.

In the general formula (1), R ¹ represents a saturated aliphatic hydrocarbon group or aromatic hydrocarbon group having 6 to 14 carbon atoms, and R ² represents a saturated aliphatic hydrocarbon group or aromatic carbon group having 1 to 10 carbon atoms. Represents a hydrogen group, and R ³ represents a saturated aliphatic hydrocarbon group or an aromatic hydrocarbon group having 1 to 12 carbon atoms. X ¹ represents a divalent group containing an oxygen atom or a sulfur atom, and X ² represents a divalent group containing a nitrogen atom, an oxygen atom or a sulfur atom. n1 represents an integer of 1 or more. When n1 is 2 or more, R ¹ and X ² that are repeated may be the same or different.

In the general formula (2), R ⁴ represents a hydrocarbon group having 6 to 30 carbon atoms. X ³ represents a divalent group containing an oxygen atom, a sulfur atom, NH or CO, and containing no hydrocarbon group at the terminal. R ⁵ represents a hydrocarbon group having 1 to 22 carbon atoms. n2 and n3 represent 0 or 1, and n2 ≧ n3.

In general formula (3), R ⁶ represents a divalent hydrocarbon group. R ⁷ represents a monovalent hydrocarbon group. X ⁴ represents a divalent linking group containing a hetero atom. n4 represents an integer of 0 to 2, and when n4 is 2, R ⁶ and X ⁴ that are repeated may be the same or different.

In general, when the reversible developer is a phenol compound having a long-chain hydrocarbon group, the compatibility with the dye precursor when heated and melted is relatively poor, and it tends to make it difficult to create a colored state with the dye. There is. The reversible developer according to the present invention has hydrocarbon groups R ¹ , R ² and R ³ , and a divalent group containing a nitrogen atom, oxygen atom or sulfur atom represented by X ² is R ¹ and is arranged between the R ^2, furthermore, the number of carbon atoms in ^{R 1} is 6 to 14. Thus, by adjusting the number of carbon atoms in R ^1, the phase of the X ² by placing the appropriate place in the hydrocarbon chain consisting of R ^1, R ^2, R ^3, the dye precursor upon heating and melting It is presumed that the solubility is improved and the color developability is improved.

  The reversible thermosensitive recording material can form a colored state and a decolored state relatively depending on the heating temperature and / or the cooling rate after heating. When the cooling rate is rapidly cooled, the reversible thermosensitive recording material forms a colored state. It can form a decolored state when it is cold. For this reason, since it is easy to shift to a rapid cooling state in a low temperature and low humidity environment, a reversible thermosensitive recording material using a conventional reversible color developer is prone to erasure defects. Erasure is caused by the phase separation of the dye precursor and the reversible developer due to crystallization of the reversible developer molecule. This facilitates the movement of the reversible developer molecule even in a low-temperature, low-humidity environment. It is important to make it easy to occur.

In the reversible developer according to the present invention, a double bond is arranged in the hydrocarbon group at the molecular end of the reversible developer represented by —R ² —CH═CH—R ³ , and further a hydrocarbon group By adjusting the carbon number of R ² and R ³ and optimizing the position of the double bond, the mobility in the reversible developer molecule increases and the reversible developer becomes easy to move. It is estimated that high-speed erasability in a low-humidity environment has been improved, and the effect has been increased by using the erasure accelerator represented by the general formula (2) or (3), and complete erasure has become possible. Conceivable.

In other words, in the present invention, by adjusting the chain length balance of the hydrocarbon group, using a reversible developer in which X ¹ and the position of the double bond are optimized, and combining a specific erasure accelerator, It is possible to obtain a reversible thermosensitive recording material that does not cause poor erasure and poor color development even under use environment conditions, particularly in a low temperature and low humidity environment, and is excellent in high color development and high-speed erasability.

  The reversible thermosensitive recording material of the present invention will be described in detail below. The reversible thermosensitive recording material of the present invention has a reversible change in color tone of the dye precursor due to the difference in heating temperature and / or the cooling rate after heating on at least one side of the support. In the reversible thermosensitive recording material provided with the reversible thermosensitive recording layer containing the reversible developer and the erasure accelerator, the phenol compound represented by the general formula (1) is used as the reversible developer. It contains at least one compound represented by formula (2) or (3) as an erasure accelerator.

In the general formula (1), R ¹ represents a saturated aliphatic hydrocarbon group or aromatic hydrocarbon group having 6 to 14 carbon atoms, and R ² represents a saturated aliphatic hydrocarbon group or aromatic carbon group having 1 to 10 carbon atoms. Represents a hydrogen group, and R ³ represents a saturated aliphatic hydrocarbon group or an aromatic hydrocarbon group having 1 to 12 carbon atoms. X ¹ represents a divalent group containing an oxygen atom or a sulfur atom, and X ² represents a divalent group containing a nitrogen atom, an oxygen atom or a sulfur atom. n1 represents an integer of 1 or more. When n1 is 2 or more, R ¹ and X ² that are repeated may be the same or different.

R ¹ represents a saturated aliphatic hydrocarbon group or aromatic hydrocarbon group having 6 to 14 carbon atoms, preferably a saturated aliphatic hydrocarbon group or aromatic hydrocarbon group having 6 to 11 carbon atoms. When the number of carbon atoms of the hydrocarbon group represented by R ¹ is smaller than 6, the color developability is lowered. This is considered to be because the compatibility between the dye precursor and the reversible developer is poor. Moreover, when the carbon number of the hydrocarbon group represented by R ¹ is larger than 14, the effect of the present invention is saturated, and the effect tends to decrease with an increase in the carbon number.

R ² represents a saturated aliphatic hydrocarbon group having 1 to 10 carbon atoms or an aromatic hydrocarbon group, preferably a saturated aliphatic hydrocarbon group having 1 to 6 carbon atoms. R ³ represents a saturated aliphatic hydrocarbon group having 1 to 12 carbon atoms or an aromatic hydrocarbon group, preferably a saturated aliphatic hydrocarbon group having 1 to 10 carbon atoms. When the number of carbon atoms in R ² exceeds 10, or when the number of carbon atoms in R ³ exceeds 12, the color developability decreases. When there is no R ² and the double bond is adjacent to the divalent group represented by X ² , the erasability deteriorates, but this is due to the intermolecular relationship between the divalent groups represented by X ^2. This is thought to be due to the stronger action. On the other hand, when there is no R ³ and the double bond is at the molecular end of the reversible developer, the erasability is also deteriorated, but this is because the mobility in the reversible developer molecule is not so great. Presumed.

In the reversible developer represented by the general formula (1), the double bond sandwiched between R ² and R ³ is preferably in a trans form. In the case of the cis form, the reversible developer molecules are bent and the strain is increased, so that the linearity of the reversible developer molecules is lost, and the cohesive force between the reversible developer molecules decreases, and the dye precursor The colored state cannot be stabilized between the body and the high colorability may not be obtained.

The sum of the carbon numbers of R ² and R ³ is preferably 5 to 14, but more preferably the sum of the carbon numbers is 5 to 10. When the sum of the carbon numbers of R ² and R ³ is smaller than 5, the erasability may be deteriorated because the cohesive force between hydrocarbon groups is weakened between the molecules of the reversible developer. On the other hand, when the sum of the carbon number of R ² and R ³ is larger than 14, contrary to the above case, the cohesive force between hydrocarbon groups becomes too strong between the molecules of the reversible developer, so May decrease.

When R ¹ , R ² , and R ³ are all saturated aliphatic hydrocarbon groups, the linearity of the reversible developer molecules increases, so that the cohesive force between the reversible developer molecules is sufficiently increased, and erasure is achieved. Improves.

In the compound represented by the general formula (1), X ¹ represents a divalent group containing an oxygen atom or a sulfur atom, preferably —CO—, —O—, —S—, —SO ₂ —. Represents a divalent group having at least one group represented by the formula: Specific examples thereof include —O—, —S—, —SO ₂ —, —CONH—, —NHCO—, —NHCOO—, —OCONH—, —NHCONH—, —CONHNHCO—, —NHCONCONH—, —CONHCONH—. , -NHCONHCO-, -OCONHCONH-, -NHCONHCOO-, -OCONHNHCO-, -CONHNHCOO-, -CONHNHCONH-, -NHCONHNHCO-, and the like. Among these, when X ¹ is —O—, it is particularly preferable because of excellent color developability.

In the compound represented by the general formula (1), X ² represents a divalent group containing a nitrogen atom, an oxygen atom, or a sulfur atom, preferably —NH—, —CO—, —O—, — S _-, - SO 2 - a group represented by a divalent group having at least 1 or more. Specific examples thereof include —NH—, —CO—, —O—, —S—, —SO ₂ —, —CONH—, —NHCO—, —NHCOO—, —OCONH—, —NHCONH—, —CONHNHCO—. , -NHCONCONH-, -CONHCONH-, -NHCONHCO-, -OCONHCONH-, -NHCONHCOO-, -OCONHNHCO-, -CONHNHCOO-, -CONHNHCONH-, -NHCONHNHCO-, and the like. Among these, -NHCONH-, -CONHNHCO-, and -NHCOCONH- are particularly preferable from the balance of color developability and erasability.

  Specific examples of the reversible developer represented by the general formula (1) are shown in Chemical Formulas 5 to 9 below, but the present invention is not limited thereto.

  A reversible color developer may be used independently and may use 2 or more types together. The amount of the reversible developer used relative to the dye precursor is 5 to 5000% by mass, preferably 10 to 3000% by mass. The reversible developer may be subjected to treatment such as microencapsulation, resin coating, and composite particle formation with resin. The dye precursor and the reversible developer may be combined and subjected to treatment such as microencapsulation, resin coating, or composite particle formation with resin.

  The reversible thermosensitive recording layer according to the present invention comprises at least one dye precursor, a reversible developer represented by the general formula (1), and an erasure accelerator represented by the general formula (2) or (3). And further contains a binder resin and other components as required. In the reversible thermosensitive recording material of the present invention, a plurality of reversible thermosensitive recording layers having different color tones may be stacked or provided on the front and back surfaces of the support. Further, the reversible thermosensitive recording layers having different color tones may be provided independently so as not to overlap each other on one surface of the support.

In the general formula (2), R ⁴ represents a hydrocarbon group having 6 to 30 carbon atoms. X ³ represents a divalent group containing an oxygen atom, a sulfur atom, NH or CO, and containing no hydrocarbon group at the terminal. R ⁵ represents a hydrocarbon group having 1 to 22 carbon atoms. n2 and n3 represent 0 or 1, and n2 ≧ n3. That is, when n2 is 0, n3 is 0, and when n2 is 1, n3 is 0 or 1.

In the general formula (2), R ⁴ represents a hydrocarbon group having 6 to 30 carbon atoms, preferably 10 to 28 carbon atoms, and more preferably 12 to 24 carbon atoms. R ⁵ represents a hydrocarbon group having 1 to 22 carbon atoms, preferably 1 to 18 carbon atoms, and more preferably 1 to 12 carbon atoms. Furthermore, the case where the sum of the carbon numbers of R ⁴ and R ⁵ is 11 or more and 35 or less is particularly preferable. R ⁴ and R ⁵ specifically represent an alkyl group and an alkylene group, respectively, but may contain an aromatic ring.

On the other hand, X ³ represents a divalent group containing an oxygen atom, a sulfur atom, NH or CO, and not containing a hydrocarbon group at the end. Specific examples thereof include —O—, —S—, —NH—. , —CO—, —COO—, —OCO—, —CONH—, —NHCO—, —NHCOO—, —OCONH—, —NHSO ₂ —, —SO ₂ NH—, —CONHCO—, —NHCONH—, —NHCSNH -, -CONHNHCO-, -NHCONCONH-, -CONHCONH-, -NHCONHCO-, -OCONHCONH-, -NHCONHCOO-, -OCONHNHCO-, -CONHNHCOO-, -NHCONHNH-, -NHNHCONH-, -CONHNHCONH-, -NHCONHNHCO-, etc. other, for example, _{-NHCOCH 2 O -, - NHCOCH 2} S-, _{OCH 2 NHCONH -, - SCH 2} NHCONH -, - CONHCH 2 NHCO -, - CONHCH 2 NHCONH -, - NHCONHCH 2 NHCO -, - NHCOCH 2 CONH -, - CONH (CH 2) 2 NHCO -, - CONH (CH 2 _{) 2 O -, - CONH (} CH 2) 2 S -, - CONH (CH 2) 2 COO -, - NHCO (CH 2) 4 CONH -, - CONH (CH 2) 6 NHCO- such as in a two Examples thereof also include a divalent group in which a valent hydrocarbon group is sandwiched between —O—, —S—, —NH—, or —CO— and an atomic group other than hydrocarbon. The atomic group other than hydrocarbon here refers to a nitrogen atom, an oxygen atom, a sulfur atom and the like and a carbon atom bonded thereto, specifically, —SS—, —NR— (R is a hydrogen atom or Alkyl group), —SO ₂ —, —CH═N—, —N═CH—, —N═N— and the like. The divalent hydrocarbon group sandwiched between NH or CO and an atomic group other than hydrocarbon preferably has 1 to 12 carbon atoms, and more preferably 1 to 6 carbon atoms. This hydrocarbon group may have a substituent. X ³ is preferably —O—, —S—, —NH—, —NHCO—, —CONH—, —NHCONH—, —CONHNHCO—, or —NHCOCONH—.

  Examples of the erasing accelerator represented by the general formula (2) are shown below, but the present invention is not limited thereto. M1, m2, and m3 represent integers that arbitrarily satisfy 5 ≦ m1 ≦ 29, 1 ≦ m2 ≦ 12, and 1 ≦ m3 ≦ 22, respectively.

CH ₃ (CH ₂ ) _m1 CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCONH ₂ , CH ₃ (CH ₂ ) _m1 NHCONCONH ₂ , CH ₃ (CH ₂ ) _m1 OCONHCONH ₂ , CH ₃ (CH ₂ ) _m1 NHNHCONH ₂ , CH ₃ (CH ₂ ) _{m 1} CONHNHCONH ₂ , CH ₃ (CH ₂ ) _{m 1} NH (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} CO (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} OCO (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 CONH (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCO (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCOO (CH _{2) m3 CONH 2, CH 3} (CH 2) m1 NHCONH (CH 2) m3 CONH 2, CH 3 (CH 2) m1 C _{NHNHCO (CH 2) m3 CONH 2} , CH 3 (CH 2) m1 NHCOCONH (CH 2) m3 CONH 2,

CH ₃ (CH ₂ ) _{m 1} NH (CH ₂ ) _{m 2} NHCO (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} NH (CH ₂ ) _{m 2} NHCONH (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _m1 NH (CH ₂ ) _m2 CONH (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NH (CH ₂ ) _m2 COO (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NH (CH ₂ ) _m2 CH═N (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NH (CH ₂ ) _m2 N═N (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 CO (CH ₂ ) _m2 NHCO (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} CO (CH ₂ ) _{m 2} NHCONH (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} CO (CH ₂ ) _{m 2} CONH (CH ₂ ) _{m 3} CO _{NH 2, CH 3 (CH 2} ) m1 CO (CH 2) m2 COO (CH 2) m3 CONH 2, CH 3 (CH 2) m1 CO (CH 2) m2 CH = N (CH 2) m3 CONH 2, CH ₃ (CH ₂ ) _{m 1} CO (CH ₂ ) _{m 2} N═N (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} CONH (CH ₂ ) _{m 2} NHCO (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _m1 CONH (CH ₂ ) _m2 NHCONH (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 CONH (CH ₂ ) _m2 CONH (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 CONH (CH ₂ ) _{) m2 COO (CH 2) m3} CONH 2, CH 3 (CH 2) m1 CONH (CH 2) m2 CH = N (CH 2) m3 CONH 2, CH 3 (CH 2) m1 CONH (CH 2) m _{N = N (CH 2) m3} CONH 2, CH 3 (CH 2) m1 NHCO (CH 2) m2 NHCO (CH 2) m3 CONH 2, CH 3 (CH 2) m1 NHCO (CH 2) m2 NHCONH (CH 2 ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCO (CH ₂ ) _m2 CONH (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCO (CH ₂ ) _m2 COO (CH ₂ ) _m3 CONH ₂ , CH _{3 (CH 2) m1 NHCO (} CH 2) m2 CH = N (CH 2) m3 CONH 2, CH 3 (CH 2) m1 NHCO (CH 2) m2 N = N (CH 2) m3 CONH 2,

CH ₃ (CH ₂ ) _{m 1} NHCOO (CH ₂ ) _{m 2} NHCO (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} NHCOO (CH ₂ ) _{m 2} NHCONH (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCOO (CH ₂ ) _m2 CONH (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCOO (CH ₂ ) _m2 COO (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCOO (CH ₂ ) _m2 CH═N (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCOO (CH ₂ ) _m2 N═N (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCONH (CH ₂ ) _m2 NHCO _{(CH 2) m3 CONH 2,} CH 3 (CH 2) m1 NHCONH (CH 2) m2 NHCONH (CH 2) m3 CONH 2, CH 3 (CH _{) M1 NHCONH (CH 2) m2} CONH (CH 2) m3 CONH 2, CH 3 (CH 2) m1 NHCONH (CH 2) m2 COO (CH 2) m3 CONH 2, CH 3 (CH 2) m1 NHCONH (CH 2 _{) m2 CH = N (CH 2} ) m3 CONH 2, CH 3 (CH 2) m1 NHCONH (CH 2) m2 N = N (CH 2) m3 CONH 2, CH 3 (CH 2) m1 NHCOCONH (CH 2) m2 NHCO (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCOCONH (CH ₂ ) _m2 NHCONH (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCONCONH (CH ₂ ) _m2 CONH (CH ₂ ) _m3 CONH ₂ , CH ₃ (CH ₂ ) _m1 NHCOCONH (CH ₂ ) _m2 COO (CH ₂ ) _m3 CONH ₂ , CH _{3 (CH 2) m1 NHCOCONH (} CH 2) m2 CH = N (CH 2) m3 CONH 2, CH 3 (CH 2) m1 NHCOCONH (CH 2) m2 N = N (CH 2) m3 CONH 2 and the like.

When X ³ contains an oxygen atom or a sulfur atom, CH ₃ (CH ₂ ) _{m 1} O (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} S (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH _{2) m1 SO 2 NH (CH} 2) m3 CONH 2, CH 3 (CH 2) m1 NHSO 2 (CH 2) m3 CONH 2, CH 3 (CH 2) m1 CONHSO 2 (CH 2) m3 CONH 2, CH 3 (CH ₂ ) _m1 NHCSNH (CH ₂ ) _m3 CONH ₂ ,

CH ₃ (CH ₂ ) _{m 1} O (CH ₂ ) _{m 2} NHCO (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} S (CH ₂ ) _{m 2} NHCO (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m1 SO 2 NH (CH 2)} m2 NHCO (CH 2) m3 CONH 2, CH 3 (CH 2) m1 NHSO 2 (CH 2) m2 NHCO (CH 2) m3 CONH 2, CH 3 (CH 2) m1 NHCO ( CH ₂ ) _{m 2} O (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} NHCO (CH ₂ ) _{m 2} S (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} NHCO (CH ₂ ) _{m 2} SS ( _{CH 2) m3 CONH 2, CH} 3 (CH 2) m1 NHCO (CH 2) m2 SO 2 (CH 2) m3 CONH 2, CH 3 (CH 2) m1 NHCO (CH 2) m2 NHCSNH (C _{2) m3 CONH 2, CH 3} (CH 2) m1 O (CH 2) m2 NHCONH (CH 2) m3 CONH 2, CH 3 (CH 2) m1 S (CH 2) m2 NHCONH (CH 2) m3 CONH 2, CH ₃ (CH ₂ ) _{m 1} SO ₂ NH (CH ₂ ) _{m 2} NHCONH (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} NHSO ₂ (CH ₂ ) _{m 2} NHCONH (CH ₂ ) _{m 3} CONH ₂ , CH ₃ ( CH ₂ ) _{m 1} NHCONH (CH ₂ ) _{m 2} O (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} NHCONH (CH ₂ ) _{m 2} S (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} NHCONH ( CH ₂ ) _{m 2} SS (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} NHCONH (CH ₂ ) _{m 2} SO ₂ (CH ₂ ) _{m 3} CONH ₂ , CH _{3 (CH 2) m1 NHCONH (} CH 2) m2 NHCSNH (CH 2) m3 CONH 2, CH 3 (CH 2) m1 O (CH 2) m2 CH = N (CH 2) m3 CONH 2, CH 3 (CH 2 ) _m1 S (CH ₂ ) _{m 2} CH═N (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH ₂ ) _{m 1} SO ₂ NH (CH ₂ ) _{m 2} CH═N (CH ₂ ) _{m 3} CONH ₂ , CH ₃ (CH _{2 ) m1 NHSO 2 (CH 2)} m2 CH = N (CH 2) m3 CONH 2 and the like.

Among the above erasing accelerators, in the present invention, when R ⁴ is a hydrocarbon group having 10 to 28 carbon atoms, further 12 to 24 carbon atoms, or X ³ (n2 = 1), —O—, —S -, -NH-, -NHCO-, -CONH-, -NHCONH-, -CONHNHCO-, -NHCOCONH-, R ⁵ is a hydrocarbon group having 0 to 12 carbon atoms (zero carbon number is n3 = 0) is preferable, and furthermore, in addition to R ⁴ , X ³ and R ⁵ satisfying these conditions, the number of atoms constituting the molecular chain of the erasure accelerator and the phenol of the reversible developer This is a case where the difference in the number of atoms constituting the chain of R ⁴ + X ³ + R ⁵ excluding the portion is ± 4.

  Furthermore, the erasure accelerator used in the present invention is a compound represented by the following general formula (3), and at least one of them is used.

In general formula (3), R ⁶ represents a divalent hydrocarbon group. R ⁷ represents a monovalent hydrocarbon group. X ⁴ represents a divalent linking group containing a hetero atom. n4 represents an integer of 0 to 2.

In the compound represented by the general formula (3), R ⁶ is preferably a divalent hydrocarbon group having 1 to 18 carbon atoms, more preferably a divalent hydrocarbon group having 1 to 12 carbon atoms. R ⁷ is preferably a monovalent hydrocarbon group having 1 to 24 carbon atoms, more preferably a hydrocarbon group having 6 to 22 carbon atoms. R ⁶ and R ⁷ are specifically an alkylene group and an alkyl group, respectively, but each group may contain an aromatic ring, but preferably only an aliphatic hydrocarbon group. On the other hand, X ⁴ represents a divalent linking group containing a hetero atom, but represents an oxygen atom, a sulfur atom, or a divalent linking group having —CONH— as the minimum structural unit. -CONH-, -NHCO-), urea (-NHCONH-), carbamic acid ester (-NHCOO-, -OCONH-), diacylamine (-CONHCO-), diacylhydrazine (-CONHNHCO-), oxalic acid diamide (- NHCONCONH-), acylurea (-CONHCONH-, -NHCONHCO-), 3-acylcarbazic acid ester (-CONHNHCOO-), semicarbazide (-NHCONHNH-, -NHNHCONH-), acyl semicarbazide (-CONHNHCONH-, -NHCONHNHCO-) ), Diacylaminomethane ( -CONHCH ₂ NHCO -), 1-acylamino-1-Ureidometan _{(-CONHCH 2 NHCONH -, - NHCONHCH} 2 NHCO-), include groups such as malonamide _(-NHCOCH 2 CONH-), preferably, an amide (- CONH-, -NHCO-), urea (-NHCONH-), diacylhydrazine (-CONHNHCO-), and oxalic acid diamide (-NHCOCONH-). n4 represents an integer of 0 to 2, but when n4 is 2, R ⁶ and X ^{4 that} are repeated may be the same or different.

  Hereinafter, preferred specific examples of the erasing accelerator represented by the general formula (3) are shown in Chemical Formula 12, but the present invention is not limited thereto.

  There is no restriction | limiting in particular as a dye precursor concerning this invention, According to the objective, it can select suitably, For example, a leuco dye etc. are mentioned suitably. As the leuco dye, a fluorane compound or an azaphthalide compound can be preferably used. Hereinafter, specific examples of the dye precursor will be given.

  2-anilino-3-methyl-6-diethylaminofluorane, 2-anilino-3-methyl-6- (di-n-butylamino) fluorane, 2-anilino-3-methyl-6- (di-n-amylamino) ) Fluorane, 2-anilino-3-methyl-6- (di-isoamylamino) fluorane, 2-anilino-3-methyl-6- (Nn-propyl-N-methylamino) fluorane, 2-anilino-3 -Methyl-6- (N-isopropyl-N-methylamino) fluorane, 2-anilino-3-methyl-6- (N-isobutyl-N-methylamino) fluorane, 2-anilino-3-methyl-6- ( Nn-amyl-N-methylamino) fluorane, 2-anilino-3-methyl-6- (N-sec-butyl-N-methylamino) fluorane, 2-anilino- -Methyl-6- (Nn-amyl-N-ethylamino) fluorane, 2-anilino-3-methyl-6- (N-isoamyl-N-ethylamino) fluorane, 2-anilino-3-methyl-6 -(Nn-propyl-N-isopropylamino) fluorane, 2-anilino-3-methyl-6- (N-cyclohexyl-N-methylamino) fluorane, 2-anilino-3-methyl-6- (N- Ethyl-p-toluidino) fluoran, 2-anilino-3-methyl-6- (N-methyl-p-toluidino) fluoran.

  2- (m-trichloromethylanilino) -3-methyl-6-diethylaminofluorane, 2- (m-trifluoromethylanilino) -3-methyl-6-diethylaminofluorane, 2- (m-trichloromethyl) Anilino) -3-methyl-6- (N-cyclohexyl-N-methylamino) fluorane, 2- (2,4-dimethylanilino) -3-methyl-6-diethylaminofluorane, 2- (2,4 -Dimethylanilino) -3-methyl-6- (di-n-butylamino) fluorane, 2- (m-toluidino) -3-methyl-6-diethylaminofluorane, 2- (m-toluidino) -3- Methyl-6- (di-n-butylamino) fluorane, 2- (p-toluidino) -3-methyl-6-diethylaminofluorane, 2- (p-toluidino) -3-me 6- (di-n-butylamino) fluorane, 2- (N-ethyl-p-toluidino) -3-methyl-6- (N-ethylanilino) fluorane, 2- (N-ethyl-p-toluidino) -3-methyl-6- (N-propyl-p-toluidino) fluorane, 2-anilino-6- (Nn-hexyl-N-ethylamino) fluorane, 2- (o-chloroanilino) -6-diethylaminofluor Oran, 2- (o-chloroanilino) -6- (di-n-butylamino) fluorane, 2- (m-trifluoromethylanilino) -6-diethylaminofluorane, 2,3-dimethyl-6-dimethylamino Fluorane, 3-methyl-6- (N-ethyl-p-toluidino) fluorane, 2-chloro-6-diethylaminofluorane.

  2-bromo-6-diethylaminofluorane, 2-chloro-6- (di-n-propylamino) fluorane, 3-chloro-6-cyclohexylaminofluorane, 3-bromo-6-cyclohexylaminofluorane, 2- Chloro-6- (N-ethyl-N-isoamylamino) fluorane, 2-chloro-3-methyl-6-diethylaminofluorane, 2-anilino-3-chloro-6-diethylaminofluorane, 2- (o-chloroanilino) ) -3-Chloro-6-cyclohexylaminofluorane, 2- (m-trifluoromethylanilino) -3-chloro-6-diethylaminofluorane, 2- (2,3-dichloroanilino) -3-chloro -6-diethylaminofluorane, 1,2-benzo-6-diethylaminofluorane, 3-diethylamino-6 (M-trifluoromethyl) -6 fluoran.

  3- (1-Ethyl-2-methylindol-3-yl) -3- (2-ethoxy-4-diethylaminophenyl) -4-azaphthalide, 3- (1-ethyl-2-methylindol-3-yl) -3- (2-Ethoxy-4-diethylaminophenyl) -7-azaphthalide, 3- (1-octyl-2-methylindol-3-yl) -3- (2-ethoxy-4-diethylaminophenyl) -4- Azaphthalide, 3- (1-ethyl-2-methylindol-3-yl) -3- (2-methyl-4-diethylaminophenyl) -4-azaphthalide, 3- (1-ethyl-2-methylindole-3- Yl) -3- (2-methyl-4-diethylaminophenyl) -7-azaphthalide, 3- (1-ethyl-2-methylindol-3-yl) -3- (4-diethyl) Aminophenyl) -4-azaphthalide, 3- (1-ethyl-2-methylindol-3-yl) -3- (4-Nn-amyl-N-methylaminophenyl) -4-azaphthalide, 3- ( 1-methyl-2-methylindol-3-yl) -3- (2-hexyloxy-4-diethylaminophenyl) -4-azaphthalide, 3,3-bis (2-ethoxy-4-diethylaminophenyl) -4- Azaphthalide, 3,3-bis (2-ethoxy-4-diethylaminophenyl) -7-azaphthalide.

  2- (p-acetylanilino) -6- (Nn-amyl-Nn-butylamino) fluorane, 2-benzylamino-6- (N-ethyl-p-toluidino) fluorane, 2-benzylamino -6- (N-methyl-2,4-dimethylanilino) fluorane, 2-benzylamino-6- (N-ethyl-2,4-dimethylanilino) fluorane, 2-benzylamino-6- (N- Methyl-p-toluidino) fluorane, 2-benzylamino-6- (N-ethyl-p-toluidino) fluorane, 2- (bis-p-methylbenzylamino) -6- (N-ethyl-p-toluidino) fluorane 2-([alpha] -phenylethylamino) -6- (N-ethyl-p-toluidino) fluorane.

  2-methylamino-6- (N-methylanilino) fluorane, 2-methylamino-6- (N-ethylanilino) fluorane, 2-methylamino-6- (Nn-propylanilino) fluorane, 2-ethylamino -6- (N-methyl-p-toluidino) fluorane, 2-methylamino-6- (N-methyl-2,4-dimethylanilino) fluorane, 2-ethylamino-6- (N-ethyl-2, 4-dimethylanilino) fluorane, 2-dimethylamino-6- (N-methylanilino) fluorane, 2-dimethylamino-6- (N-ethylanilino) fluorane, 2-diethylamino-6- (N-methyl-p-toluidino ) Fluorane, 2-diethylamino-6- (N-ethyl-p-toluidino) fluorane, 2-di-n-propylamino-6- N- methylanilino) fluoran, 2-di -n- propyl amino-6-(N- ethylanilino) fluoran.

  2-amino-6- (N-methylanilino) fluorane, 2-amino-6- (N-ethylanilino) fluorane, 2-amino-6- (Nn-propylanilino) fluorane, 2-amino-6- ( N-methyl-p-toluidino) fluorane, 2-amino-6- (N-ethyl-p-toluidino) fluorane, 2-amino-6- (Nn-propyl-p-toluidino) fluorane, 2-amino- 6- (N-methyl-p-ethylanilino) fluorane, 2-amino-6- (N-ethyl-p-ethylanilino) fluorane, 2-amino-6- (Nn-propyl-p-ethylanilino) fluorane, 2 -Amino-6- (N-methyl-2,4-dimethylanilino) fluorane, 2-amino-6- (N-ethyl-2,4-dimethylanilino) fluorane, 2 Amino-6- (Nn-propyl-2,4-dimethylanilino) fluorane, 2-amino-6- (N-methyl-p-chloroanilino) fluorane, 2-amino-6- (N-ethyl-p -Chloroanilino) fluorane, 2-amino-6- (Nn-propyl-p-chloroanilino) fluorane, 1,2-benzo-6- (N-ethyl-N-isoamylamino) fluorane, 1,2-benzo- 6- (Di-n-butylamino) fluorane, 1,2-benzo-6- (N-methyl-N-cyclohexylamino) fluorane, 1,2-benzo-6- (N-ethyl-p-toluidino) fluorane .

  4,4'-bis (dimethylaminophenyl) benzhydrylbenzyl ether, N-chlorophenyl leucooramine, N-2,4,5-trichlorophenyl leucooramine, benzoyl leucomethylene blue, p-nitrobenzoyl leucomethylene blue, 3 -Methylspirodinaphthopyrans, 3-ethylspirodinaphthopyrans, 3,3'-dichlorospirodinaphthopyrans, 3-benzylspirodinaphthopyrans, 3-methylnaphthyl (3-methoxybenzo) spiropyrans, 3-propylspiros Benzopyran.

  These dye precursors may be used singly or in combination of two or more. Toning can also be performed by mixing dye precursors that develop colors in other hues. In addition, a multicolor reversible thermosensitive recording material or a full-color reversible thermosensitive recording material can be obtained by laminating layers that develop colors of different colors or arranging them on a plane. The dye precursor may be subjected to processing such as microencapsulation, resin coating, and composite particle formation with a resin.

  The support according to the present invention includes paper, non-woven fabric / woven fabric / knitted fabric, plastic film, resin-coated paper, synthetic paper, metal plate, metal foil, glass, quartz glass, silicon resin, aluminum oxide, silicon oxide Etc., or a combination of these can be arbitrarily used depending on the purpose. Examples of the plastic film that can be used in the present invention include polyester film, polyolefin film, polyvinyl alcohol film, polyvinyl chloride film, nylon film, polystyrene film, polyvinylidene chloride film, ethylene-vinyl acetate copolymer film, ethylene-vinyl. Examples include alcohol copolymer films, fluororesin films, polyimide films, aromatic polyamide films, acrylic (based) resin films, and polycarbonate films. A polyester film is preferable in terms of mechanical strength, smoothness, water resistance, solvent resistance, and heat resistance. These synthetic resin materials may be used alone or in combination of two or more.

  Examples of the polyester film include polyethylene terephthalate (PET), polybutylene terephthalate, poly-1,4-cyclohexanedimethylene terephthalate, polyxylylene terephthalate, polyethylene isophthalate, polyethylene-2,6-naphthalate (PEN). It is done. Preferred polyester films include PET films or PEN films that are excellent in toughness, heat resistance, chemical resistance, dimensional stability, transparency, and electrical insulation.

  The support may be opaque, translucent or transparent. In order to make the background appear white or other specific colors, a white pigment, a colored dye pigment, or air bubbles may be included in the support or on the surface. When the reversible thermosensitive recording layer is coated on the support with low affinity, it can be applied to the support surface by corona discharge treatment, oxidation reaction treatment (chromic acid, etc.), etching treatment, easy adhesion treatment, antistatic treatment, etc. The modification treatment may be performed. There is no restriction | limiting in particular about a shape, a structure, a magnitude | size, etc. as a support body concerning this invention. Examples of the shape include a flat plate shape and a roll shape. The structure may be a single layer structure or a laminated structure, and the size can be appropriately selected according to the use of the reversible thermosensitive recording material.

  The thickness of the support according to the present invention can be appropriately selected according to the use of the reversible thermosensitive recording material, but is preferably 10 to 2000 μm, and more preferably 20 to 1000 μm.

  The reversible thermosensitive recording layer according to the present invention is formed by applying and forming a reversible thermosensitive recording layer coating solution containing at least a dye precursor and a reversible developer on at least one surface of a support. The As a method for including the dye precursor and the reversible developer in the reversible thermosensitive recording layer coating liquid, each compound is dissolved in a solvent alone or dispersed in a dispersion medium and then mixed. Are mixed in a solvent and then dissolved in a solvent or dispersed in a dispersion medium, and each compound is heated and dissolved, homogenized and then cooled, and then dissolved in a solvent or dispersed in a dispersion medium. It is not a thing. If necessary, a dispersing agent may be used during dispersion.

  As a solvent or dispersion medium, water; alcohols such as methanol, ethanol, n-propanol, 2-propanol (isopropyl alcohol) and n-butanol; ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone and isophorone; acetic acid Esters such as methyl, ethyl acetate, butyl acetate, isobutyl acetate, isopropyl acetate, ethyl lactate, ethylene carbonate, ethers such as diethyl ether, glycol dimethyl ether, glycol diethyl ether, dioxane, tetrahydrofuran, benzene, toluene, xylene, cresol, Aromatic hydrocarbons such as styrene; aliphatic hydrocarbons such as pentane, hexane and cyclohexane; methylene chloride, ethylene chloride, carbon tetrachloride, Chloroform, ethylene chlorohydrin, chlorobenzene, halogenated hydrocarbons such as dichlorobenzene; N, N- dimethylformamide, N, etc. amides such as N- dimethylacetamide can be used.

  For the purpose of improving the strength of the reversible thermosensitive recording layer, a binder resin can be added to the reversible thermosensitive recording layer. Specific examples of the binder resin include starches, hydroxyethyl cellulose, methyl cellulose, carboxymethyl cellulose, gelatin, casein, polyvinyl alcohol, modified polyvinyl alcohol, polyacrylic acid soda, (meth) acrylic acid amide- (meth) acrylic acid ester copolymer Polymer, (meth) acrylic acid amide- (meth) acrylic acid ester- (meth) acrylic acid terpolymer, alkali salt of styrene-maleic anhydride copolymer, alkali salt of ethylene-maleic anhydride copolymer , Polyvinyl acetate, polyurethane, poly (meth) acrylic acid ester, styrene-butadiene copolymer, acrylonitrile-butadiene copolymer, methyl (meth) acrylate-butadiene copolymer, ethylene-vinyl acetate copolymer, ethylene -PVC Alcohol copolymer, polyvinyl chloride, ethylene - vinylidene chloride copolymer, polyvinylidene chloride, polycarbonates, polyvinyl butyral, and the like. The role of these binder resins is to keep the materials contained in the reversible thermosensitive recording layer uniformly dispersed without being displaced by heat application for image recording or image erasing. Therefore, it is preferable to use a resin having high heat resistance as the binder resin. When heat resistance, water resistance, and adhesiveness are required, a curable resin is particularly preferable.

  Examples of the curable resin include a thermosetting resin, an electron beam curable resin, and an ultraviolet curable resin. When a thermosetting resin is applied, a liquid containing a crosslinking agent is applied and formed into a film, and then crosslinked by heat. Specific examples of the thermosetting resin include epoxy resins, urea resins, xylene-formaldehyde resins, melamine resins, guanamine resins, phenol resins, phenoxy resins, saturated polyester resins, unsaturated polyester resins, and polyol resins. Curing agents used in these thermosetting resins include organic acids, amines, isocyanates, epoxies, phenols, etc., but select a suitable reactive agent depending on the type of thermosetting resin. Just do it. Among these, a crosslinked resin obtained by thermosetting a polyol compound with an isocyanate compound described in JP-A-10-230680 and JP-A-11-58963 is preferable.

  As oligomers / monomers used for electron beam curable resins or UV curable resins, there are many types of acrylic oligomers / monomers with excellent radiation curing properties, polyene-thiol oligomers / monomers, and photocationic polymerization type epoxy. Examples include oligomers and monomers. Examples of the acrylic monomer include a monofunctional monomer, a bifunctional monomer, and a polyfunctional monomer. In particular, a photopolymerization initiator and a photopolymerization accelerator are used at the time of ultraviolet crosslinking.

  Examples of the acrylic oligomer / monomer include polyester acrylate, polyether acrylate, epoxy acrylate, polyurethane acrylate, silicone acrylate, melamine acrylate, polybutadiene acrylate, and the like.

  In the reversible thermosensitive recording layer according to the present invention, a binder resin formed by crosslinking a polyol compound and an isocyanate compound, which is a preferable binder resin, will be described. Examples of the polyol compound include poly (meth) acryl polyol, polyester polyol, polycarbonate polyol, polyester polycarbonate polyol, polyether polyol, alkyd polyol, caprolactone polyol, and silicone polyol.

  Poly (meth) acrylic polyol is a copolymer of acrylic acid, methacrylic acid and esters thereof, which contains a hydroxyl group, and the copolymer component containing a hydroxyl group includes hydroxyethyl acrylate, methacrylic acid. Hydroxyethyl acid, hydroxypropyl acrylate, hydroxypropyl methacrylate, 3-chloro-2-hydroxypropyl acrylate, 3-chloro-2-hydroxypropyl methacrylate, allyl alcohol and the like are used. Examples of copolymer components other than acrylic acid, methacrylic acid and esters thereof include styrene, α-methylstyrene, vinyltoluene, acrylamide, methacrylamide and derivatives thereof, vinyl acetate, maleic anhydride and the like.

  Polyester polyol refers to a condensate of a polybasic acid and a polyhydric alcohol having a hydroxyl group. Polybasic acids used in these are phthalic acid, isophthalic acid, terephthalic acid, trimellitic acid. , Aromatic polybasic acids such as trimesic acid, pyromellitic acid, naphthalenedicarboxylic acid, oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, dodecanedioic acid, 2-methylsuccinic acid, 2-methyladipic acid, 3-methyladipic acid, 3-methylpentanedioic acid, 2-methyloctanedioic acid, 3,7-dimethyldecanedioic acid, 3,8-dimethyldecanedioic acid, There are aliphatic polybasic acids such as dimer acid, and acid anhydrides obtained from these polybasic acids are also used.

  Polyhydric alcohols include ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, propanediol, neopentyl glycol, glycerin, trimethylolethane, trimethylolpropane, diglycerol, pentaerythritol, dipentaerythritol, di In addition to low molecular weight polyols such as acetone glycol and hexanetriol, high molecular weight polyols such as polyethylene glycol, polypropylene glycol and polybutylene glycol are also used. In addition to polyester polyols obtained from these, hydroxycarboxylic acids, or condensates or ring-opening polymerizations of cyclic lactones thereof, such as polybutyrolactone polyols, polycaprolactone polyols, and higher fatty acids in addition to the above polybasic acids and polyhydric alcohols. There are alkyd polyols obtained by condensation. The polyether polyol is a polymer having a main chain composed of an ether bond, and includes polyethylene glycol, polypropylene glycol, polybutylene glycol, and these branched esters.

  Examples of polyether polyols include ethylene oxide and / or propylene oxide adducts of polyhydric alcohols, polytetramethylene glycol, and the like. Examples of the silicone polyol include silicone oils having a siloxane bond in the molecule and a terminal hydroxyl group.

  In addition, fluorine-containing polyols such as hydroxyl-containing fluoroolefin, polyol hydroxyl-terminated polybutadiene, polyisoprene, hydrogenated polybutadiene, hydrogenated polyisoprene, polyurethane and the like can be used. Further, low molecular weight polyols such as diethylene glycol, triethylene glycol, glycerol, trimethylolpropane, pentaerythritol, 1,4-cyclohexadiol, 1,4-dihydroxybenzene, bisphenol A, bisphenol F, and other aliphatic, fatty A cyclic, aromatic polyhydric alcohol or polyhydric phenol or a condensate thereof is used as a reactive diluent.

  As the polyol compound according to the present invention, poly (meth) acrylic polyol and polyester polyol are preferable from the comprehensive evaluation of additive dispersibility, coating property, adhesiveness, heat resistance and film strength. The polyol compound according to the present invention may be used singly or in combination with one or more other polyol compounds having different structures of the polyol part and other parts, or having different molecular weights.

  A well-known thing can be used as an isocyanate compound concerning this invention. For example, aromatic aliphatic diisocyanates such as phenylene diisocyanate (PDI), toluene diisocyanate (TDI), naphthalene diisocyanate (NDI), 4,4'-diphenylmethane diisocyanate (MDI), xylylene diisocyanate (XDI), hydrogenated TDI, water Aliphatic or alicyclic diisocyanates such as hydrogenated XDI, hydrogenated MDI, hexamethylene diisocyanate (HDI), isophorone diisocyanate (IPDI) and their derivatives, polyol adducts, burette bodies, trifunctional or more trifunctional or higher functional groups. In addition to polyisocyanate, various oligomers and polymers containing isocyanate may be mentioned. In the present invention, when xylylene diisocyanate or toluene isocyanate is used as the isocyanate compound, the color density is preferably improved, and further, xylylene diisocyanate having a high background whiteness is more preferable.

  The isocyanate compound according to the present invention may be used alone or in combination with two or more isocyanates with respect to one or more polyol compounds. In the case where a plurality of isocyanate compounds and polyol compounds are used, the combination may be arbitrary.

  The mixture of the polyol compound and the polyisocyanate compound may be used as it is when they are in liquid form, but can also be used after diluted with a non-reactive solvent with the polyisocyanate compound. As the solvent that can be used, a solvent that dissolves the polyol compound and the polyisocyanate compound and disperses and dissolves the dye precursor and the reversible developer is preferable. Specifically, the solvents exemplified in the method for incorporating the dye precursor and the reversible developer into the reversible thermosensitive recording layer coating liquid can be used. Among them, it is preferable to use an organic solvent that does not have active hydrogen that is reactive with the polyisocyanate compound. The crosslinking reaction between the polyol compound and the polyisocyanate compound may be performed at a reaction temperature of 30 to 160 ° C. and a reaction time of 1 minute to 120 hours. Needless to say, it takes a long time when the reaction temperature is low, and a short time at a high temperature.

  The amount of the binder resin used in the reversible thermosensitive recording layer according to the present invention is preferably in the range of 35 to 65% by mass, more preferably 40 to 60% by mass with respect to the total mass of the reversible thermosensitive recording layer. 45 to 55% by mass is preferable. If it exceeds 65% by mass, the color density may decrease significantly. On the contrary, if it is less than 35% by mass, the heat resistance and mechanical strength of the reversible thermosensitive recording layer may be reduced, the layer may be deformed, and the color density may be reduced.

  A binder resin can be added to the reversible thermosensitive recording layer, if necessary. Further, for the purpose of improving coating properties or recording characteristics, a leveling agent, a dispersant, a hardener, a surface active agent can be used. Agent, thickener, antifoaming agent, antioxidant, anti-aging agent, filler, pigment, lubricant, antistatic agent, ultraviolet absorber, infrared absorber, colored dye / pigment, fluorescent whitening agent, thermofusible substance Further, an antiseptic and the like can be contained in the reversible thermosensitive recording layer.

  When the reversible thermosensitive recording layer contains a curable resin, heating, ultraviolet irradiation, and electron beam irradiation are performed. Ultraviolet irradiation can be performed using a known ultraviolet irradiation device, and examples thereof include a light source, a lamp, a power source, a cooling device, and a conveying device. Examples of the light source include a mercury lamp, a metal halide lamp, a gallium lamp, a mercury xenon lamp, and a flash lamp. The wavelength of the light source can be appropriately selected according to the ultraviolet absorption wavelength of the photopolymerization initiator and the photopolymerization accelerator. The output and conveying speed of the ultraviolet irradiation are determined according to the irradiation energy necessary for crosslinking the ultraviolet curable resin.

  Anti-aging agents added for the purpose of preventing aging of the reversible thermosensitive recording layer include amine compounds such as p, p'-diaminodiphenylmethane, aldol-α-naphthylamine, and N, N'-diphenyl-p-phenylenediamine. , Hydroquinone monobenzyl ether, phenol compounds such as 1,1-bis (p-hydroxyphenyl) cyclohexane, benzotriazole compounds, triazine compounds, benzophenone compounds, benzoates and the like. In addition, o-phenylenethiourea, zinc salt of 2-aminobenzimidazole, nickel dibutylthiocarbamate, zinc oxide, paraffin and the like can be mentioned. In addition, a polymer containing these monomers having an anti-aging structure as a component of polymerization, and a polymer main chain grafted with an anti-aging structure can also be used. Two or more types of anti-aging agents can be used in combination.

  Examples of pigments that can be added to the reversible thermosensitive recording layer include, for example, carbonates such as aluminum, zinc, calcium, magnesium, barium, and titanium, oxides, hydroxides, sulfates, etc., and zeolite, silica, Inorganic pigments containing clays such as kaolin, calcined kaolin and talc, starch, styrene resin, polyolefin resin, urea-formalin resin, melamine resin, acrylic resin, paraffin, natural wax, synthetic wax and the like can be used. Further, higher fatty acid metal salts such as zinc stearate and calcium stearate can be used as a lubricant.

  The film thickness of the reversible thermosensitive recording layer is arbitrarily determined depending on the composition of the reversible thermosensitive recording layer and the desired color density, but is preferably 0.5 to 20 μm, and preferably 3 to 15 μm. More preferred.

  In the reversible thermosensitive recording material of the present invention, it is preferable to provide a protective layer on the reversible thermosensitive recording layer for the purpose of enhancing durability during repeated use. The protective layer may be composed of a single layer or a plurality of layers of two layers or three or more layers. The protective layer preferably contains a curable resin such as a thermosetting resin, an electron beam curable resin, or an ultraviolet curable resin, and particularly preferably an electron beam curable resin or an ultraviolet curable resin. As the curable resin, resins exemplified as binder resins that can be used in the reversible thermosensitive recording layer can be used. Further, for the purpose of further improving the durability or adjusting the glossiness, a pigment may be blended, or a higher fatty acid metal salt may be blended as a lubricant. As the pigment and the higher fatty acid metal salt, the compounds exemplified in the reversible thermosensitive recording layer can be used.

  The thickness of the protective layer is preferably in the range of 0.1 to 10 μm, more preferably 0.5 to 5 μm. When the film thickness exceeds 10 μm, not only the effect is saturated, but also the sensitivity of the reversible thermosensitive recording layer tends to decrease. When the film thickness is smaller than 0.1 μm, it is difficult to obtain the expected coating layer strength, and the coating layer is easily damaged.

  In the present invention, an intermediate layer is provided between the reversible thermosensitive recording layer and the protective layer for the purpose of improving weather resistance, etc., an undercoat layer is provided for the purpose of improving color development sensitivity, etc., a light reflecting layer and an air layer are provided. May be. The intermediate layer may contain an ultraviolet absorber. Further, when the reversible thermosensitive recording layer is provided only on one side of the support, a back coat layer may be provided on the other side. Examples of the ultraviolet absorber include a benzophenone ultraviolet absorber, a benzotriazole ultraviolet absorber, and a salicylic acid phenyl ester ultraviolet absorber. The undercoat layer may contain hollow particles. These layers may be composed of a single layer or a plurality of layers of two layers or three or more layers. Moreover, it is preferable that these layers contain curable resins, such as a thermosetting resin, an electron beam curable resin, and an ultraviolet curable resin.

  In the present invention, a leveling agent, a dispersant, a hardener, a surfactant, a thickener, a hardener is optionally added to the protective layer, intermediate layer, undercoat layer and the like provided on the support. Various additives such as preservatives, fillers, coloring dyes, fluorescent brighteners, UV absorbers, infrared absorbers, antioxidants, antioxidants, pH regulators, antifoaming agents, pigments, lubricants, antistatic agents An agent can be added.

  The reversible thermosensitive recording material of the present invention may be provided with a printing recording layer such as printing such as offset printing or gravure printing; an ink jet recording layer, a thermal transfer image receiving layer, a sublimation thermal transfer image receiving layer. These printing and print recording layers may be provided by being laminated with the reversible thermosensitive recording layer, or may be provided on a part of the same surface as the reversible thermosensitive recording layer. Further, it may be provided on a part of or the entire surface opposite to the surface on which the reversible thermosensitive recording layer is provided. An overprint varnish (OP varnish) layer mainly composed of a curable resin may be provided partially or entirely on the print recording layer.

  In the reversible thermosensitive recording material of the present invention, in the reversible thermosensitive recording layer, other layers, the surface provided with the reversible thermosensitive recording layer, the opposite surface, etc. are electrically, magnetically and optically information. May contain a recordable material. Further, the support may be a multilayer and an IC chip may be sandwiched between them. Further, an antistatic layer can be provided on one side or both sides for the purpose of antistatic. The reversible thermosensitive recording material of the present invention can be attached to another medium through an adhesive layer or the like or using a heat-fusible resin as a support.

  When the IC chip is encapsulated between the layers of the reversible thermosensitive recording material, for example, it can be encapsulated between the layers of the plastic film or between the paper substrate and the plastic film. It is preferable from the viewpoint of print quality that sealing is performed between layers away from the reversible thermosensitive recording layer. When enclosing a non-contact IC chip, it can be encapsulated together with an antenna. A cushion layer can be provided for the purpose of preventing the IC chip from being damaged by the pressure during encapsulation. The thickness of the cushion layer is preferably 10 μm or more because cushioning properties are insufficient if it is less than 10 μm. In addition, since a load is applied to the joint between the IC chip and the antenna, the area of the cushion layer is preferably large enough to cover the IC chip and the antenna joint. The cushion layer can be provided on one side or both sides. More preferably, cushion layers are provided on both sides. As the cushion layer, a thermoplastic resin is preferable. The foamed resin has better cushioning properties and can prevent the IC chip from being damaged.

  A method for forming the reversible thermosensitive recording material by coating the reversible thermosensitive recording layer and other layers on the support is not particularly limited. For example, an air knife coater, a blade coater, a bar coater, a curtain coater, Gravure roll and transfer roll coater, roll coater, comma coater, smoothing coater, micro gravure coater, reverse roll coater, 4 or 5 roll coater, dip coater, rod coater, kiss coater, gate roll coater, squeeze coater, slide coater, A smearing device such as a die coater, a flat plate, a letterpress, an intaglio, a flexo, a gravure, a screen, and various printing machines such as a hot melt can be used. Further, in addition to a normal drying step, each layer can be held by ultraviolet irradiation or electron beam irradiation. By these methods, it is possible to apply and print one layer at a time or multiple layers simultaneously.

  In the reversible thermosensitive recording material of the present invention, rapid cooling is required following heating to form a color-recorded recording image, and a slow cooling rate after heating is sufficient to erase the recorded image. For example, after heating by an appropriate method, a colored state can be developed by rapidly cooling by pressing a low-temperature metal block or the like. In addition, if the heating is performed for a very short time using a thermal head, laser light, or the like, the cooling is performed immediately after the heating is completed, so that the colored state can be maintained. On the other hand, when heated for a relatively long time with a suitable heat source (thermal head, laser light, heat roll, heat stamp, high-frequency heating, electric heater, radiant heat from a light source such as a tungsten lamp or halogen lamp, hot air, etc.) Since not only the layer but also the support and the like are heated, even if the heat source is removed, the cooling rate is slow, and the color is lost. Therefore, even when the same heating temperature and the same heat source are used, the coloring state and the decoloring state can be arbitrarily expressed by controlling the cooling rate.

  Examples of the laser used for heating include, but are not limited to, a semiconductor laser, a YAG laser, and a carbon dioxide gas laser. For efficient heating with a semiconductor laser or YAG laser, a reversible thermosensitive recording layer contains a photothermal conversion material having absorption in the near infrared region, or a photothermal conversion layer containing a photothermal conversion material is reversible. It is preferably provided directly adjacent to the heat-sensitive recording layer. Examples of photothermal conversion materials having absorption in the near infrared region include, for example, metal or metalloid layers such as platinum, titanium, silicon, chromium, nickel, germanium, and aluminum, immonium compounds, metal complex compounds, cyanine dyes, squarylium dyes, Examples thereof include, but are not limited to, naphthoquinone dyes, phthalocyanine compounds, and naphthalocyanine compounds.

  Hereinafter, the present invention will be described with reference to examples. The present invention is not limited to these examples. In the examples, the number of parts and percentage are based on mass unless otherwise specified.

Synthesis example 1
<Reversible developer: Synthesis of trans form in which double bond sandwiched between R ₂ and R ₃ in exemplary compound (1-13)>

  A reaction vessel was charged with 10.0 g of 4- (benzyloxy) phenol, 14.0 g of methyl 11-bromoundecanoate, 8.5 g of potassium carbonate, and 80 ml of N, N-dimethylformamide (DMF) at 100 ° C. for 5 hours. Stir and react. After cooling the reaction solution to room temperature, water was added. The precipitated crystals were separated by filtration, washed with water and dried to obtain crystals of methyl 11-[(4-benzyloxy) phenoxy] undecanoate. Along with the obtained methyl 11-[(4-benzyloxy) phenoxy] undecanoate, 0.3 g of palladium carbon (5%) and 300 ml of ethanol were charged in a reaction vessel, and stirred at 60 ° C. under a hydrogen stream for 24 hours. Deprotection (debenzylation) reaction was performed. After the palladium carbon was filtered off, the filtrate was charged into a reaction vessel together with 5 g of hydrazine monohydrate and reacted for 24 hours under reflux. After cooling the reaction solution to room temperature, the precipitated crystals were separated by filtration, washed with water and dried to obtain 11- (4-hydroxyphenoxy) undecanoic acid hydrazide crystals. The obtained 11- (4-hydroxyphenoxy) undecanoic acid hydrazide was charged into a reaction vessel together with 4.1 g of trans-4-decenoic acid, 4.0 g of N, N′-diisopropylcarbodiimide and 150 ml of tetrahydrofuran, and reacted for 5 hours under reflux. I let you. After cooling the reaction solution to room temperature, the crystals obtained after filtration and washing with methanol were recrystallized from 2-propanol to obtain 11.0 g of the desired product. The melting point was 167 ° C.

Example 1
(1) Preparation of reversible thermosensitive recording layer coating solution 20 parts of 2-anilino-3-methyl-6- (di-n-butylamino) fluorane as a dye precursor and R ² and R ³ as a reversible developer 100 parts of Exemplified Compound (1-13) obtained in Synthesis Example 1 in which the sandwiched double bond is in trans form, 10 parts of behenamide as an erasing accelerator, polyester polyol (trade name “Takelac U-21”, Non-volatile content 70%, acid value <4.2, resin OH value 350 mgKOH / g, 100 parts of Mitsui Chemicals Polyurethanes Co., Ltd.), and a mixture of 950 parts of methyl ethyl ketone as a solvent are dispersed in a paint shaker for 24 hours together with glass beads. Got. To this dispersion, 144 parts of an isocyanate compound (trade name “Takenate D-110N”, non-volatile content 75%, manufactured by Mitsui Chemicals Polyurethane Co., Ltd.) was added and mixed well to prepare a reversible thermosensitive recording layer coating solution.

(2) Preparation of intermediate layer coating solution 50 parts of UV absorber (trade name “Tinubin 328”, manufactured by Ciba Specialty Chemicals Co., Ltd.), polyester polyol (trade name “Bernock 11-408”, nonvolatile content 70%, A mixture of 100 parts of DIC Corporation and 800 parts of methyl ethyl ketone was dispersed with a glass bead for 5 hours with a paint shaker to obtain a dispersion. 140 parts of an isocyanate compound (trade name “Takenate D-110N”, non-volatile content 75%, manufactured by Mitsui Chemicals Polyurethane Co., Ltd.) and 50 parts of methyl ethyl ketone are added to the dispersion thus obtained and mixed well to prepare an intermediate layer coating liquid. did.

(3) Preparation of coating liquid for protective layer 100 parts of urethane acrylate ultraviolet curable resin (trade name “Unidic V-4205”, manufactured by DIC Corporation), silica particles having an average particle diameter of 1.2 μm (trade name “Nip Seal”) SS-50F ”(manufactured by Tosoh Silica Co., Ltd.) 10 parts and 90 parts of isopropyl alcohol were mixed well to prepare a protective layer coating solution.

(4) Production of reversible thermosensitive recording material The reversible thermosensitive recording layer coating liquid obtained in (1) was applied to a white polyethylene terephthalate (PET) sheet having a thickness of 188 μm so that the dry film thickness was 8 μm. After drying at 120 ° C. for 1 minute, the mixture was further heated at 50 ° C. for 48 hours to form a reversible thermosensitive recording layer. On the reversible thermosensitive recording layer, the intermediate layer coating solution obtained in (2) was applied so that the dry film thickness was 1 μm, dried at 120 ° C. for 1 minute, and further heated at 50 ° C. for 48 hours. An intermediate layer was formed. After coating the protective layer coating solution obtained in (3) on the intermediate layer, the coating is cured by passing it under a UV lamp with an irradiation energy of 80 W / cm ² at a conveyance speed of 9 m / min. A 3 μm protective layer was provided to obtain a reversible thermosensitive recording material of the present invention.

Example 2
In Example 1, a reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1 except that stearic acid amide was used instead of behenic acid amide.

Example 3
In Example 1, a reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1, except that lauric acid amide was used instead of behenic acid amide.

Example 4
In Example 1, the reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1 except that 6-n-octadecylthiohexanoic acid amide was used instead of behenamide as the erasure accelerator. .

Example 5
In Example 1, the reversible thermosensitive composition of the present invention was used in the same manner as in Example 1 except that 8- (n-octadecylaminocarbonylamino) -octanoic acid amide was used instead of behenic acid amide as the erasure accelerator. A recording material was obtained.

Example 6
In Example 1, the reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1 except that the example accelerator (3-1) was used instead of behenamide as the erasure accelerator.

Example 7
In Example 1, the reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1 except that the exemplified compound (3-3) was used instead of behenamide as the erasure accelerator.

Example 8
In Example 1, a reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1, except that the exemplified compound (3-5) was used instead of behenamide as the erasure accelerator.

Example 9
In Example 1, a reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1, except that the exemplified compound (3-6) was used instead of behenamide as the erasure accelerator.

Example 10
In Example 1, a reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1, except that the exemplified compound (3-8) was used instead of behenamide as the erasure accelerator.

Example 11
In Example 1, the double bond which is sandwiched between the reversible color developer in R ² and R ³ in place of the exemplified compound is a trans form (1-13), a double bond sandwiched R ² and R ³ A reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1 except that the exemplified compound (1-5) in a trans form was used.

Example 12
In Example 1, the double bond which is sandwiched between the reversible color developer in R ² and R ³ in place of the exemplified compound is a trans form (1-13), a double bond sandwiched R ² and R ³ A reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1 except that the exemplified compound (1-6) in a trans form was used.

Example 13
In Example 1, the double bond which is sandwiched between the reversible color developer in R ² and R ³ in place of the exemplified compound is a trans form (1-13), a double bond sandwiched R ² and R ³ A reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1 except that the exemplified compound (1-7) in trans form was used.

Example 14
In Example 1, the double bond which is sandwiched between the reversible color developer in R ² and R ³ in place of the exemplified compound is a trans form (1-13), a double bond sandwiched R ² and R ³ A reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1 except that the exemplified compound (1-8) in trans form was used.

Example 15
In Example 1, the double bond which is sandwiched between the reversible color developer in R ² and R ³ in place of the exemplified compound is a trans form (1-13), a double bond sandwiched R ² and R ³ A reversible thermosensitive recording material of the present invention was obtained in the same manner as in Example 1 except that the exemplified compound (1-9) in a trans form was used.

Comparative Example 1
In Example 1, a reversible thermosensitive recording material was obtained in the same manner as in Example 1 except that behenamide was not used as the erasure accelerator.

Comparative Example 2
In Example 1, a reversible thermosensitive recording material was obtained in the same manner as in Example 1 except that the example accelerator (4-1) was used instead of behenamide as the erasure accelerator.

Comparative Example 3
In Example 1, a reversible thermosensitive recording material was obtained in the same manner as in Example 1 except that the exemplified compound (4-2) was used instead of behenamide as the erasure accelerator.

Comparative Example 4
In Example 1, a reversible thermosensitive recording material was obtained in the same manner as in Example 1 except that the exemplified compound (4-3) was used instead of behenamide as the erasure accelerator.

  The following evaluation was performed on the reversible thermosensitive recording materials obtained in Examples 1 to 15 and Comparative Examples 1 to 4.

Evaluation 1: Print Erase Test of Reversible Thermosensitive Recording Material Applied to a reversible thermosensitive recording material using an Okura Electric thermal facsimile printing tester TH-PMD with a Kyocera print head KJT-256-8MGF1. Printing is performed at an applied voltage of 26 volts in milliseconds, and the color is erased at 120 ° C. for 0.5 seconds using a thermal inclination tester manufactured by Toyo Seiki Co., Ltd., and the optical density of the printed portion, erased portion and background portion is determined. It was measured with a Macbeth densitometer RD-918. This was printed and erased in an environment of normal temperature and normal humidity (20 ° C., 50% RH) and low temperature and low humidity (5 ° C., 30% RH). For the erasability, the density of the background portion was subtracted from the density of the erased portion, and the value was regarded as unerased. The results are shown in Table 1.

Evaluation 2: Card printer print erasure test of reversible thermosensitive recording material After forming a color image on a reversible thermosensitive recording material using a card printer (R3000 manufactured by Panasonic Communications), erase by changing the pulse width of the printer The optical density of the printed portion, erased portion and background portion was measured with a Macbeth densitometer RD-918. This was printed and erased in an environment of normal temperature and normal humidity (20 ° C., 50% RH) and low temperature and low humidity (5 ° C., 30% RH). For the erasability, the density of the background portion was subtracted from the density of the erased portion, and the value was regarded as unerased. The results are shown in Table 2.

  The reversible thermosensitive recording materials of Comparative Examples 1 to 4 had a higher decolorization density in a low temperature and low humidity (5 ° C., 30% RH) environment than in a normal temperature and normal humidity (20 ° C., 50% RH) environment. On the other hand, the reversible thermosensitive recording materials of Examples 1 to 15 are hardly affected by temperature and humidity, have almost no disappearance in both a normal temperature and normal humidity environment and a low temperature and low humidity environment, and have a higher color density. The background density was also low and high image contrast was maintained. Further, in the print erasure test using the card printer of Evaluation 2, the reversible thermosensitive recording materials of Examples 1 to 15 were in a normal temperature and normal humidity (20 ° C., 50% RH) environment and low temperature and low humidity (5 ° C., 30%). It was a reversible thermosensitive recording material with almost no disappearance in both RH) environments and excellent in high-speed decoloring properties.

  In Comparative Example 1, some unerased residue was observed, and in the print erasure test using the card printer of Evaluation 2, the unerased residue was even greater. In Comparative Examples 2, 3, and 4, the color density was low and disappearance remained, and the effect of using a specific erasure accelerator was observed.

Claims (1)

In a reversible thermosensitive recording material provided on a support with a dye precursor, a reversible developer that causes a reversible color change in the dye precursor, and a reversible thermosensitive recording layer containing an erasure accelerator, The reversible developer contains a phenol compound represented by the general formula (1), and contains at least one compound represented by the general formula (2) or (3) as the erasure accelerator. A reversible thermosensitive recording material.

(In the general formula (1), R ¹ represents a saturated aliphatic hydrocarbon group or aromatic hydrocarbon group having 6 to 14 carbon atoms, and R ² represents a saturated aliphatic hydrocarbon group or aromatic group having 1 to 10 carbon atoms. Represents a hydrocarbon group, R ³ represents a saturated aliphatic hydrocarbon group or an aromatic hydrocarbon group having 1 to 12 carbon atoms, X ¹ represents a divalent group containing an oxygen atom or a sulfur atom, and X ² represents Represents a divalent group containing a nitrogen atom, an oxygen atom, or a sulfur atom, and n1 represents an integer of 1 or more.)

(In the general formula (2), R ⁴ represents a hydrocarbon group having 6 to 30 carbon atoms. X ³ contains an oxygen atom, a sulfur atom, NH or CO, and does not contain a hydrocarbon group at the terminal. R ⁵ represents a hydrocarbon group having 1 to 22 carbon atoms, n2 and n3 represent 0 or 1, and n2 ≧ n3.

(In General Formula (3), R ⁶ represents a divalent hydrocarbon group. R ⁷ represents a monovalent hydrocarbon group. X ⁴ represents a divalent linking group containing a hetero atom. N4 represents 0. Represents an integer of ~ 2)