• 대한치과보철학회지
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• 제41권6호
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• pp.732-746
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• 2003

Statement of problem. Soft lining materials, also referred to as tissue conditioning materials, tissue heating materials, relining materials, soft liners or tissue conditioners, were first introduced to dentistry by a plastic manufacturer in 1959. Since the introduction of the materials to the dental field, their material properties have been continually improved through the effort of many researchers. Soft lining materials have become widely accepted, particularly by prosthodontists, because of their numerous clinical advantages and ease of manipulation. Unfortunately, few reports have been issued upon the topic of increasing the bond strength between the base metal alloy used in cast denture bases and PMMA soft liner modified with 4-META, nor upon the pattern of debonding and material change in wet environment like a intra oral situation. Purpose. The purposes of this study were comparing the bond strength between base metal alloy used for the cast denture bases and PMMA soft liner modified with 4-META, and describing the pattern of debonding and material property change in wet environment like the intraoral situation. Material and Methods. This study consisted of four experiments: 1. The in vitro measurement of shear bond strength of the adhesive soft liner. 2. The in vitro measurement of shear bond strength of the adhesive soft liner after 2 weeks of aging. 3. A comparison of debonding patterns. 4. An evaluation the Relation time of modified soft liner. The soft liner used in this study was commercially available as Coe-soft (GC America.IL.,USA), which is provided in forms of powder and liquid. This is a PMMA soft liner commonly used in dental clinics. The metal primer used in this study was 4-META containing primer packed in Meta fast denture base resin (Sun Medical Co., Osaka, Japan). The specimens were formed in a single lap joint desist which is useful for evaluating the apparent shear bond strength of adhesively bonded metal plate by tensile loading. Using the $20{\times}20mm$ transparent grid, percent area of adhesive soft liner remaining on the shear area was calculated to classify the debonding patterns. To evaluate the change of the initial flow of the modified adhesive soft liner, the gelation time was measured with an oscillating rheometer (Haake RS150W/ TC50, Haake Co., Germany). It was a stress control and parallel plate type with the diameter of 35mm. Conclusion. Within the conditions and limitations of this study, the following conclusions were drawn as follows. 1. There was significant increase of bond strength in the 5% 4-META, 10% 4-META containing groups and in the primer coated groups versus the control group(P<0.05). 2. After 2 weeks of aging, no significant increase in bond strength was found except for the group containing 10% 4-META (P<0.05). 3. The gelation times of the modified soft liner were 9.3 minutes for the 5% 4-META containing liner and 11.5 minutes for the 10% 4-META liner. 4. The debonding patterns of the 4-META containing group after 2 weeks of aging were similar to those of immediaely after preparation, but the debonding pattern of the primer group showed more adhesive failure after 2 weeks of aging.

• 한국재료학회지
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• 제2권3호
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• pp.220-227
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• 1992

전기유변유체(electrorheological fluid : ERF)는 크기가 $10^{-6}m$정도를 가진 분극성이 강한 입자 분말을 유전유체속에 혼합하여 만든 콜로이드용액으로서 외부전기 장에 의하여 액체상태로부터 겔(gel)상태로 상태변환을 한다. 상태변환과정은 가역과정이며 $10^{-3}$초 정도의 빠른 시간내에 이루어진다. 본 논문에서는 주기적응력이나 주기적 변형이 가해지는 강제진동실험을 통하여 ERF의 점탄성 특성을 조사하였다. 점탄성은 복소수로서 실수부인 동적전단탄성율(storage shear modulus, G')과 허수부인 동적손실율(loss modulus, G")의 합으로 표현된다. 동적전단탄성율은 강제진동의 진폭과 주파수의 함수로 외부전기장에 의하여 크게 변화되었으나 손실계수(loss factor, ${\eta}=G"/G'$)는 진동의 진폭, 진동수 및 외부전기 장에 거의 독립적이었다. 실험(1)은 강제진동의 진폭을 고정하고 진동수를 변화하는 방법(frequency sweep)과 실험(2)는 진동 진폭을 변화시키는 방법(amplitude sweep)으로 실행했다. 본 실험에서는 cornstarch입자를 corn oil에 혼합한 것과 zeolite입자를 silicone oil에 흔합한 콜로이드 용액이 ERF로서 사용되었으며 인가된 전기장은 약$(1~3){\times}10^6V/m$의 직류전기장이 가하여졌다.기장이 가하여졌다.

• Elastomers and Composites
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• 제20권1호
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• pp.13-24
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• 1985

It is generally agreed that strong linkages exist between rubber chains and reinforcing filler particles. The purpose of this study is to examine the effect of rubber-filler attachments on the various mechanical properties of the rubber. In particular, the modulus and strength will be altered by these attachments. For this study, the curing properties are examined by means of ODR (Oscillating Disk Rheometer), the physical properties by means of Instrong. The results of this study can be summarized as follows. In the ODR test, the carbon black filled stock has shorter scorch time than gum stock and, the silica and clay filled stock has longer scorch time than gum stock. In the modulus, ten sile and swelling properties, the vulcanizates filled with carbon black had higher those values than inorganic filler loaded NR vulcanizates, but the rebound rate showed that the silica filled NR vulcanizates was lower than other inorganic filler contained NR vulcanizates and the ISAF filled NR vulcanizates was lower than other carbon block contained NR vulcanizates.

• 한국염색가공학회지
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• 제33권4호
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• pp.317-326
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• 2021

In this study, we investigated for Bio-EPDM foam with oyster shell surface modified earth coupling agent. Experiments were carried out to confirm the bio-EPDM/Oyster shell foam applying content of earth coupling agent. The cure characterization were evaluated by measuring the mooney viscosity and oscillating disc rheometer (ODR). Mechanical properties such as hardness, tensile strength, elogation at break and tear strength were measured, and changes of mechanical properties were also evaluated after immersion in NaCl solution. In addition degree of volume change was measured after immersing the Bio-EPDM foam in NaCl solution and the low-temperature permanent compression set was evaluated at 4℃. To evaluate the low-temperature characteristics of Bio-EPDM/Oyster shell, the glass transition temperature was measured using Differential Scanning Calorimeter (DSC). As a result as the content of the earth coupling agent increased up to 3phr, the crosslinking density and mooney viscosity increased, and the mechanical properties and low-temperature permanent compression set improved, but from 4phr, it was rather decreased. The change in the glass transition temperature was insignificant, and the foam cell appeared to be uniform when the earth coupling agent was applied.

• 한국염색가공학회지
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• 제35권4호
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• pp.246-255
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• 2023

In this study, we investigated for natural rubber foam to replace petrochemical-based neoprene foam. Experiments were conducted on vulcanization system and 2-step foaming process of natural rubber. The vulcanization system were EV(Efficient Vulcanization Cure), Semi-EV(Semi-Efficient Vulcanization Cure) and CV(Conventional Vulcanization Cure). In the 2-step foaming process, first molding temperature was 140℃, times were 15, 20, 25, and 30minutes, and the second molding temperature was 160℃, the times 5, 10, 15, and 20minutes. The cure and viscosity characterization were evaluated by oscillating disc rheometer (ODR) and mooney viscosmeter. Various mechanical characteristics, including hardness, tensile strength, elongation at the point of rupture, and tear strength, were quantified. Subsequently, an assessment of alterations in these mechanical attributes was conducted post-immersion in a NaCl solution. In addition degree of volume change was measured after immersing the NR foam in NaCl solution and the low-temperature permanent compression set was evaluated at 4℃. And expansion ratio and shrinkage ratio of NR foam were evaluated for 28 days. As a result the EV vulcanization system showed the least change in physical properties before and after salt water immersion, and the lowest shrinkage ratio for 28 days. In addition it was confirmed that the 2-step foaming optimum condition differed depending on the appropriate vulcanization condition.

• Elastomers and Composites
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• 제19권1호
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• pp.13-31
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• 1984

The purposes of this dissertation are to demonstrate that DSC theromoanaytical methods of vulcanization can provide useful informations on the vulcanization characteristics of industrial formulations and also provides the potential basis for a rapid and complete method of sulfur and vulcanizing accelerator analysis for quality control. The influences of those factors such as heating rate, scan temperature, vucanizing accelerator's type and concentration upon vulcanization exotherm in NR and NBR compounds in the presence of vulcanizing accelerators such as TMTD,MBTS,DPG,TMTM,CBS, and MBT were evaluated by means of DSC. In order to examine the credibility in the DSC method, the same samples which were used for DSC method were studied to compare the DSC results with the ODR (Oscillating Disk Rheometer) data. The results obtained were as follows 1. In the DSC dynamic experiments, the observed enthalpy results from vulcanization depends upon the heating rate; In the range of 2 to $20^{\circ}C/min$ of heating rate, as the heating rate was increased the enthalpy change was also increased. However, over the heating rate of $30^{\circ}C/min$ it was observed that the enthalpy change was decreased as the heating rate was further increased. Without regard to the change of enthalpy, tremendous instantaneous heat evolving was observed in the range of high heating rates. 2. For the samples which are added with various vulcanizing accelerators, the activation energies of vulcanization were as follows; 3. Regarding to the influences of vulcanizining accelerator's types upon the characteristics of vulcanization exotherm, NR and NBR compounds in the presence of thiuramsulphide compounds type accelerators such as TMTD, TMTM, were exhibited sharper and higher vulclanization exotherm than others. From the resuts of DSC thermograms which was distributed in even shape in the broad temperature range, it was clearly shown that the guanidine compounds type accelerator such as DPG acts as a delayed acting accelerator. 4. In the comparison of DSC and ODR results, the dependency of temperature in the cure rate and the observed conversions show good agreements between two results. 5. In the same curatives, by the comparison of glass transition temperatures, it was possible to predict relative values of maximum torques. Consequently, from the present studies, it is shown that the DSC thermoanalytical method can provide an alternate new method for rapid and complete quality control analysis of rubber industry.

• Elastomers and Composites
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• 제22권3호
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• pp.204-212
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• 1987

본(本) 실험(實驗)에서는 고무탄성체(彈性體)에 대(對)한 무기계(無機系) 충전제(充塡劑)의 보강(補强)을 충전제(充塡劑)의 입자표면(粒子表面)과 고무분자간(分子間)의 상호작용(相互作用)에 의(依)한 화학적(化學的) 결합(結合) 측면(測面)에서 유리단섬유(短纖維) 충전(充塡)에 의(依)한 Chloroprene 고무 가황체(加黃體)의 보강효과(補强效果)를 향상(向上)시킬 목적(目的)으로 분쇄(分碎)한 유리단섬유(短纖維)($L{\fallingdotseq}30.4{\mu}m,\;d=4{\mu}m$)에 silane coupling제(劑)로 표면처리(表面處理)하여 얻어진 복합체(複合體)를 배합(配合)한 가황계(加黃系)의 가황특성(加黃特性) 및 물리적(物理的) 성질(性質)을 검토(檢討)하였다. 또한 APS배합(配合) CR 미가교체(末架橋體)를 대기중(大氣中)에 폭로(暴露)함으로서 APS에 의(依)한 후가교반응(後架橋反應)을 검토(檢討)하여 다음과 같은 결론(結論)을 얻었다. 1. ODR에 나타난 각(各) 가황계(加黃系)의 적정가황시간(適正加黃時間)($t_{90}$)은 MGF 충전(充塡)의 APS배합(配合) 가황계(架黃系)의 MC가 가장 빠르며 MGF배합(配合) 미가교체(未架橋體) AM이 가장 느렸다. 그리고 silane coupling 처리(處理) MGF는 미처리(未處理) MGF보다 최대(最大) torque값이 더 크고 적정가황시간(適正加黃時間)이 빨랐다. 2. 물리적(物理的) 성질(性質)에 있어서는 인장강도(引張强度), 인장응력(引張應力)이 SC가 가장 좋았으며, 유효강목쇄농도(有效綱目鎖濃度) 역시 SC가 가장 큰 값을 나타냈다. Silane coupling제(劑) 처리(處理) MGF는 미처리(未處理) 및 배합(配合) MGF보다 물리적(物理的) 성질(性質)과 유효강목쇄농도(有效綱目鎖濃度)가 모두 우수하였다. 3. 열노화(熱老化)에 의(依)한 물리적(物理的) 성질(性質)의 변화(變化)는 silica 충전(充塡)에서 $70^{\circ}C$, 72hr 노화시간(老化時間)을 전후(前後)하여 인장강도(引張强度), 인장응력(引張應力), 유효강목쇄농도(有效綱目鎖濃度)가 증가(增加), 감소(減少)하였으며 silane coupling제(劑) 처리(處理) MGF의 경우는 미처리(未處理) 및 배합(配合) MGF와는 달리 silica 충전계(充塡系)와 비슷한 특성(特性)을 나타내었다. 4. CR+APS+MGF와 CR+APS+silica의 미가교체(未架橋體)는 대기폭로(大氣暴露)에 의(依)한 시간(時間)의 경과에 따라 가교반응(架橋反應)이 진행(進行)되어 가교체(架橋體)의 유효강목쇄농도(有效綱目鎖濃度)와 인장물성(引張物性)이 증가(增加)되었다.