JP2015191198A5 - - Google Patents
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- JP2015191198A5 JP2015191198A5 JP2014070170A JP2014070170A JP2015191198A5 JP 2015191198 A5 JP2015191198 A5 JP 2015191198A5 JP 2014070170 A JP2014070170 A JP 2014070170A JP 2014070170 A JP2014070170 A JP 2014070170A JP 2015191198 A5 JP2015191198 A5 JP 2015191198A5
- Authority
- JP
- Japan
- Prior art keywords
- carbon dioxide
- solvent
- mass
- binder resin
- index
- 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.)
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- CURLTUGMZLYLDI-UHFFFAOYSA-N carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims 15
- 229910002092 carbon dioxide Inorganic materials 0.000 claims 15
- 239000001569 carbon dioxide Substances 0.000 claims 15
- 239000011347 resin Substances 0.000 claims 15
- 229920005989 resin Polymers 0.000 claims 15
- 239000002904 solvent Substances 0.000 claims 15
- 239000011230 binding agent Substances 0.000 claims 10
- 238000011156 evaluation Methods 0.000 claims 10
- 238000004519 manufacturing process Methods 0.000 claims 7
- 230000035515 penetration Effects 0.000 claims 5
- WVDDGKGOMKODPV-UHFFFAOYSA-N benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims 3
- 238000004090 dissolution Methods 0.000 claims 3
- 238000002844 melting Methods 0.000 claims 3
- IWDCLRJOBJJRNH-UHFFFAOYSA-N P-Cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 claims 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N Phenethyl alcohol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 claims 2
- 239000007788 liquid Substances 0.000 claims 2
- CFBYEGUGFPZCNF-UHFFFAOYSA-N 2-nitroanisole Chemical compound COC1=CC=CC=C1[N+]([O-])=O CFBYEGUGFPZCNF-UHFFFAOYSA-N 0.000 claims 1
- OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 claims 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-Methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 claims 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 1
- 235000019445 benzyl alcohol Nutrition 0.000 claims 1
- 238000009835 boiling Methods 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- 239000002612 dispersion media Substances 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- 238000005191 phase separation Methods 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
Claims (7)
b)前記樹脂溶液と、分散剤及び液体状態又は超臨界状態の二酸化炭素を含有する分散媒体とを混合し、造粒することにより前記樹脂溶液の液滴を形成する工程、及び
c)前記液滴に含まれる前記溶媒を除去してトナー粒子を得る工程、
を有するトナーの製造方法であって、
下記[評価手法1]によって求められる前記結着樹脂の通過率Aが、90.0%以上であり、
下記[評価手法2]によって求められる前記溶媒に対する二酸化炭素の溶け込み指数Bが、40.0質量%以下であり、かつ、下記[評価手法3]によって求められる二酸化炭素に対する前記溶媒の溶け出し指数Cが、2.0質量%以上20.0質量%以下であることを特徴とするトナーの製造方法。
[評価手法1]
予め粉砕した結着樹脂を篩にかけた時、目開き150μmの篩を通過し、かつ、目開き38μmの篩を通過しない結着樹脂を評価用結着樹脂として、前記評価用結着樹脂の質量をW1(g)とする。
次に、前記評価用結着樹脂を温度25℃、圧力6.5MPaの二酸化炭素と2時間混合した後、再度、目開き150μmの篩にかけて、通過した結着樹脂の質量をW2(g)とする。
前記W1及び前記W2の値から、下記式(1)によって通過率Aを求める。
通過率A(%)=W2/W1×100 (1)
[評価手法2]
密閉容器に溶媒をV1(g)投入する。次に、温度25℃で二酸化炭素を前記溶媒に対して飽和に達するまで、大気圧から加圧しながら導入し、この時の二酸化炭素の導入量をV2(g)とする。
前記溶媒と前記溶媒に飽和した二酸化炭素の総量に対する前記溶媒に飽和した二酸化炭素の含有率を溶け込み指数Bとし、前記V1及びV2の値から、下記式(2)によって、溶け込み指数Bを求める。
溶け込み指数B(質量%)=V2/(V1+V2)×100 (2)
[評価手法3]
前記[評価手法2]における溶け込み指数Bの評価後、さらに二酸化炭素を温度25℃
で圧力6.5MPaまで導入して、溶媒相と二酸化炭素相に相分離させ、この時追加導入された二酸化炭素の導入量をX1(g)とする。
前記溶媒相から、前記二酸化炭素相に移行した二酸化炭素の質量をX2(g)、前記二酸化炭素相に移行した溶媒の質量をX3(g)とする。
前記二酸化炭素相における溶媒の含有率を溶け出し指数Cとし、前記X1,X2,X3の値から下記式(3)によって溶け出し指数Cを求める。
溶け出し指数C(質量%)=X3/(X1+X2+X3)×100 (3) a) a step of mixing a binder resin and a solvent capable of dissolving the binder resin to prepare a resin solution;
b) mixing the resin solution with a dispersant and a dispersion medium containing carbon dioxide in a liquid state or supercritical state, and granulating the mixture to form droplets of the resin solution; and c) the liquid Removing the solvent contained in the droplets to obtain toner particles;
A method for producing a toner comprising:
The passing rate A of the binder resin obtained by the following [Evaluation technique 1] is 90.0% or more,
The solubility index B of carbon dioxide with respect to the solvent obtained by the following [Evaluation Method 2] is 40.0% by mass or less, and the dissolution index C of the solvent with respect to carbon dioxide obtained by the following [Evaluation Method 3]. Is 2.0% by mass or more and 20.0% by mass or less.
[Evaluation Method 1]
When the pre-ground binder resin is sieved, the mass of the evaluation binder resin is defined as a binder resin that passes through a sieve having an opening of 150 μm and does not pass through a sieve having an opening of 38 μm. Is W1 (g).
Next, after the binder resin for evaluation was mixed with carbon dioxide having a temperature of 25 ° C. and a pressure of 6.5 MPa for 2 hours, it was passed through a sieve having an opening of 150 μm again, and the mass of the binder resin passed through was determined as W2 (g). To do.
From the values of W1 and W2, the passage rate A is obtained by the following equation (1).
Passing rate A (%) = W2 / W1 × 100 (1)
[Evaluation Method 2]
V1 (g) of the solvent is put into the sealed container. Next, carbon dioxide is introduced while being pressurized from atmospheric pressure at a temperature of 25 ° C. until saturation with respect to the solvent, and the amount of carbon dioxide introduced at this time is defined as V2 (g).
The content of carbon dioxide saturated in the solvent relative to the total amount of the solvent and carbon dioxide saturated in the solvent is defined as a penetration index B, and the penetration index B is obtained from the values of V1 and V2 by the following formula (2).
Penetration index B (mass%) = V2 / (V1 + V2) × 100 (2)
[Evaluation Method 3]
After the evaluation of the penetration index B in [Evaluation Method 2], carbon dioxide was further added at a temperature of 25 ° C.
The pressure is introduced to 6.5 MPa and phase separation is carried out into a solvent phase and a carbon dioxide phase, and the amount of carbon dioxide additionally introduced at this time is X1 (g).
Let X2 (g) be the mass of carbon dioxide transferred from the solvent phase to the carbon dioxide phase, and X3 (g) be the mass of solvent transferred to the carbon dioxide phase.
The solvent content in the carbon dioxide phase is taken as the dissolution index C, and the dissolution index C is determined from the values of X1, X2, and X3 by the following formula (3).
Melting index C (mass%) = X3 / (X1 + X2 + X3) × 100 (3)
前記結晶構造を取り得る部位の含有量が結着樹脂を基準として50.0質量%以上90.0質量%以下である請求項6に記載のトナーの製造方法。 The resin containing a part capable of taking a crystal structure is a block polymer in which a part that can take a crystal structure and a part that cannot take a crystal structure are chemically bonded,
The method for producing a toner according to claim 6 , wherein the content of the portion capable of taking the crystal structure is 50.0% by mass or more and 90.0% by mass or less based on the binder resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014070170A JP6272105B2 (en) | 2014-03-28 | 2014-03-28 | Toner production method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014070170A JP6272105B2 (en) | 2014-03-28 | 2014-03-28 | Toner production method |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2015191198A JP2015191198A (en) | 2015-11-02 |
JP2015191198A5 true JP2015191198A5 (en) | 2017-04-13 |
JP6272105B2 JP6272105B2 (en) | 2018-01-31 |
Family
ID=54425704
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2014070170A Active JP6272105B2 (en) | 2014-03-28 | 2014-03-28 | Toner production method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP6272105B2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9798256B2 (en) * | 2015-06-30 | 2017-10-24 | Canon Kabushiki Kaisha | Method of producing toner |
JP6562821B2 (en) * | 2015-11-20 | 2019-08-21 | キヤノン株式会社 | Resin particle manufacturing method and toner manufacturing method |
JP2018124317A (en) * | 2017-01-30 | 2018-08-09 | コニカミノルタ株式会社 | Toner for electrostatic charge image development, two-component developer for electrostatic charge image development, and method for manufacturing toner for electrostatic charge image development |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5005730B2 (en) * | 2008-05-23 | 2012-08-22 | 三洋化成工業株式会社 | Resin particles and method for producing the same |
TWI461864B (en) * | 2011-06-03 | 2014-11-21 | Canon Kk | Toner |
JP5773764B2 (en) * | 2011-06-03 | 2015-09-02 | キヤノン株式会社 | Toner production method |
JP2013155210A (en) * | 2012-01-26 | 2013-08-15 | Sanyo Chem Ind Ltd | Core-shell type resin particle, and method for manufacturing the same |
JP2014038169A (en) * | 2012-08-14 | 2014-02-27 | Ricoh Co Ltd | Production method of toner, and toner |
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2014
- 2014-03-28 JP JP2014070170A patent/JP6272105B2/en active Active
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