Продукты

Carbon Printers FotoDent IBT Methacrylate resin

    • Название продукта: Carbon Printers FotoDent IBT Methacrylate resin
    • Сайт Factroy: Округ Юду, Ганьчжоу, Цзянси, Китай
    • Запрос цены: admin@ascent-chem.com
    • Производитель: Ascent Petrochem Holdings Co., Limited
    • Свяжитесь сейчас
    Спецификации
    Код ТН ВЭД 912540

    Как аккредитованный завод по производству метакрилатной смолы FotoDent IBT, мы соблюдаем строгие протоколы качества - каждая партия подвергается строгим испытаниям для обеспечения последовательных стандартов эффективности и безопасности.

    Упаковка и хранение
    Упаковка Carbon Printers FotoDent IBT Methacrylate resin is supplied in a sealed, light-resistant 1 kg bottle with safety labels.
    Погрузка контейнера (20-футовый контейнер) Container Loading (20′ FCL) of Carbon Printers FotoDent IBT Methacrylate resin: palletized, secured, kept upright, away from heat and ignition.
    Доставка Carbon Printers FotoDent IBT Methacrylate resin ships in sealed, labeled original containers. Consult the SDS; many methacrylate resins are not DOT/IATA dangerous goods, but classification can vary. Keep cool, dry, upright, away from sunlight and ignition. Use PPE and spill containment. Follow all applicable local, national, and international shipping regulations.
    Хранение Store Carbon Printers FotoDent IBT Methacrylate resin in its original, tightly sealed container in a cool, dry, well-ventilated area. Protect from direct sunlight, heat, sparks, flames, and incompatible materials such as oxidizers and amines. Maintain recommended temperature, typically 15–25°C, and observe shelf-life. Keep away from food, drink, and children; use appropriate PPE and spill containment.
    Срок годности Shelf life: approximately 24 months from manufacture when stored unopened at 15–25°C, protected from light, heat, and moisture.
    Применение углеродных принтеров FotoDent IBT метакрилатная смола

    Carbon Printers FotoDent IBT methacrylate resin is used in full-arch labial bracket transfer tray production as a single-component photopolymer; no chemical mixing ratio is required before loading into the printer cassette. The resin is formulated for the Carbon DLS oxygen-permeable membrane process, where the dead zone at the build interface suppresses layer-by-layer delamination and produces a more isotropic green part than conventional stereolithography. In the digital setup for a full-arch labial transfer tray, each bracket base is imported from intraoral scan software, and the tray body is offset from the bracket base by 0.30 mm to 0.50 mm. This geometric ratio creates the adhesive space that controls final bond line thickness after the tray is seated. The tray body is assigned a wall thickness of 1.5 mm over the facial surfaces, while occlusal stops are extruded to 2.0 mm height. During printing, the arch is oriented with the occlusal plane rotated 30° to 45° relative to the build platform, which reduces the cross-sectional area of each printed layer and lowers the separation force at the resin-membrane interface. After the build is complete, the green part is removed from the build platform, and residual resin is washed from bracket slots and internal voids in 99% isopropanol for 2 min in an ultrasonic bath set to 30°C. Oil-free compressed air at 0.2 MPa is used to remove solvent from the bracket slots. The tray is then post-cured in a 405 nm LED chamber for 5 min per side, with the device rotated between sides to avoid localized overheating. Terminal product is a semi-rigid full-arch tray that seats on the occlusal stops and transfers the bracket slots with a dimensional tolerance of ±0.10 mm relative to the digital setup. Compliance for transient mucosal contact is evaluated under ISO 10993-1:2018; the resin manufacturer's technical file typically includes ISO 10993-5:2009 cytotoxicity and ISO 10993-10:2021 sensitization data. Laboratories that run high-volume production should verify lot consistency by printing a reference tray and measuring bracket slot width, because batch-to-batch variation in methacrylate resin viscosity can shift the effective layer thickness. Use of amine-based accelerators in the indirect bonding adhesive should be controlled, because tertiary amines may interact with residual methacrylate on the tray surface and promote premature gelation at the adhesive-tray interface.

    Standard or test methodRelevant clause or designationApplication to indirect bonding tray resin
    ISO 10993-1:2018Biological evaluation of medical devicesContact duration classification for transient oral use
    ISO 10993-5:2009In vitro cytotoxicityExtractable leachables from post-cured resin
    ISO 10993-10:2021Skin sensitization and irritationMucosal irritation potential of tray surface
    ISO 178:2019Flexural propertiesBending stiffness under seating load
    ISO 868:2003Shore D hardnessRapid batch check of cured resin

    Why Lingual Indirect Bonding Demands a Different Tray Geometry?

    On lingual surfaces, transfer trays made from the same FotoDent IBT methacrylate resin are not geometrically equivalent to labial trays. The interbracket distance on the lingual surface is smaller, and the palatal insertion path requires a more rigid tray body to prevent distortion during bracket transfer. The digital offset between the lingual bracket base and the tray is reduced to 0.20 mm to 0.30 mm because excess adhesive is difficult to remove from the lingual embrasures and can interfere with centric contacts. Tray body thickness is increased to 2.0 mm in the anterior palatal region, and posterior occlusal stops are widened to 3.0 mm to distribute seating pressure. These ratios are not arbitrary; they compensate for the lower effective stiffness of the palatal extension under finger loading. Flexural modulus is measured by ISO 178:2019 three-point bending, and published data for this specific resin configuration is limited, so laboratories should perform lot-level verification with at least 5 specimens per ISO 178:2019 sampling protocols. Build orientation is shifted to a more vertical arrangement with the incisal edge upward and the palatal surface facing the build platform at approximately 60°. This orientation reduces the number of support contact points that would otherwise leave surface blemishes on the bracket slot walls. Post-cure is performed at 405 nm for 10 min per side in a nitrogen-purged LED chamber; the nitrogen blanket suppresses atmospheric oxygen inhibition and increases surface conversion. The terminal product is a lingual tray with palatal finger rests and a posterior seating stop that does not rock on the occlusal surface. A relief of 0.05 mm is applied to the palatal soft-tissue area to reduce mucosal blanching during insertion. If the tray is subjected to cleaning, only pH-neutral non-solvent disinfectants are used, because alkaline cleaners may hydrolyze methacrylate ester groups and induce microcracking. In batch production, trays with visible layering or incomplete fusion in the palatal extension are rejected before delivery because the insertion path magnifies any interlayer weakness.

    In segmental rebonding workflows, Carbon Printers FotoDent IBT methacrylate resin serves a different function than full-arch transfer trays. When only one or two brackets require repositioning, segmental coverage reduces seating variability and allows direct visual confirmation of bracket position. The digital setup spans 2 to 4 adjacent teeth, and the tray wall over the replacement bracket is thickened to 2.5 mm to resist local flexure. The adhesive offset is set to 0.25 mm to 0.35 mm, while the occlusal stop is reduced to 1.5 mm height to minimize occlusal interference during light-cure. The resin is processed as a single-component system without monomer dilution; addition of external methacrylate monomers is prohibited because changing the crosslink density shifts the gel point and increases the extractable fraction. The segment is printed at 50 µm layer height to preserve fine bracket slot detail. After printing, the guide is washed in two sequential baths of 99% isopropanol for 1.5 min per bath; the first bath removes bulk liquid resin, and the second bath removes the residual smear layer. The part is air-dried and post-cured in a nitrogen-purged 405 nm LED chamber for 10 min. Because the guide is small, the nitrogen atmosphere has a measurable effect on surface conversion; the oxygen-inhibited layer at the top surface is reduced, and the bracket slot shows less residual tack. The final sectional guide is seated with light finger pressure, and the bracket slot is inspected for flash under magnification. Visible interlayer delamination or slot deformation beyond 0.10 mm is cause for rejection. This application does not require a full-arch seating path, so the main process risk is local bending stress during bracket release. The guide is therefore treated as a single-use transfer device unless a validated cleaning protocol is in place.

    When Chairside Same-Day Printing Replaces Laboratory Transfer Trays

    In chairside production environments, the elapsed time from intraoral scan to seated transfer tray is commonly compressed to 45–60 min, which changes the selection of layer height and post-cure equipment. The resin cassette is preheated to the printer's operating temperature range of 30°C to 35°C to stabilize methacrylate viscosity; below 25°C viscosity increases enough to alter recoating dynamics and reduce dimensional accuracy. A layer height of 100 µm is selected for full-arch trays when speed is prioritized, while 50 µm is reserved for segmental guides or cases with narrow bracket slots. The chairside post-cure step may use a handheld LED curing box for 3 min per surface, but this shorter cycle may not achieve the same conversion as a laboratory nitrogen-purged chamber. To compensate for green-state dimensional drift during same-day handling, the digital tray is designed with an additional 0.10 mm adhesive offset beyond the standard 0.30 mm to 0.50 mm. The terminal product must reproduce bracket slot positions within ±0.15 mm relative to the approved digital setup. If the printed tray does not seat passively, it is rejected and reprinted rather than adjusted by grinding. Grinding removes the crosslinked surface skin and exposes partially polymerized methacrylate domains, which can irritate oral mucosa and weaken the transfer interface. Compliance in a chairside setting is procedural: the clinic must use the manufacturer-validated print profile for FotoDent IBT on the specific Carbon printer model and must not mix the resin with other methacrylate photopolymers. Photoinitiator concentration, oxygen inhibition behavior, and post-cure response differ between resin formulations, so cross-contamination can produce unpredictably soft trays or brittle bracket slots. Rapid lot checks using Shore D hardness per ISO 868:2003 may be used, but the acceptance range must be derived from the resin manufacturer's stated post-cure values rather than generic dental acrylic tables.

    Thermal and Solvent Tolerance During Post-Cure and Disinfection

    For post-cure validation of FotoDent IBT methacrylate resin, solvent tolerance and thermal ageing under clinical disinfection define the operational boundary of the final indirect bonding tray. In orthodontic practice, trays may be wiped with 70% ethanol or 2% glutaraldehyde after chairside try-in. Methacrylate networks with incomplete conversion are susceptible to solvent-induced microcracking, particularly at the edges of bracket slots where crosslink density is lower. The wash step before final cure is therefore critical: an ultrasonic bath of 99% isopropanol at 30°C for 2 min removes uncured resin from recesses, while cold solvent increases the viscosity of the residual monomer film and slows dissolution. Drying with oil-free compressed air at 0.2 MPa prevents solvent pooling in the bracket slots. Post-cure in a 405 nm LED chamber for 10 min per side under nitrogen reduces the oxygen-inhibited layer and improves solvent resistance of the tray surface. Autoclaving of methacrylate trays is not recommended unless the specific printed configuration has been validated by thermal cycling, because expansion at 121°C may create interfacial stress between polymerized layers and cause dimensional shift in the bracket slot. Published data on autoclave reuse of this specific resin is limited; therefore, the default operational boundary is a single-use tray that is disinfected with a solvent wipe rather than heat-sterilized. If a dental facility chooses to reuse an indirect bonding tray, it must perform its own biological evaluation under ISO 10993-1:2018 and verify that repeated solvent exposure does not reduce flexural modulus below the lot threshold established by ISO 178:2019 testing. High-volume dental laboratories should also monitor ambient humidity: methacrylate resins are hygroscopic before cure, and exposure to relative humidity above 60% can increase water absorption in the green part, leading to post-cure warpage. The terminal product is a dry, solvent-resistant tray with stable bracket slot geometry after one disinfection cycle; any sign of surface tack, whitening, or interlayer separation is grounds for rejection before delivery to the clinic.

    Бесплатная цитата

    Конкурентные углеродные принтеры FotoDent IBT цены на метакрилатную смолу, которые соответствуют вашему бюджету - гибкие условия и индивидуальные котировки для каждого заказа.

    Для получения образцов, цен или более подробной информации свяжитесь с нами по адресу +8618136850665 или отправить по почте admin@ascent-chem.com.

    Мы ответим вам как можно скорее.

    Телефон: +8618136850665

    Электронная почта: admin@ascent-chem.com

    Запрос

    Получите бесплатную сметуAscent Petrochem Holdings Co., Limited

    Гибкие условия оплаты, конкурентоспособные цены, первоклассное обслуживание — обращайтесь прямо сейчас!

    Сертификация и соответствие требованиям
    Более подробное введение

    Carbon Printers FotoDent IBT Methacrylate resin is a light-curable methacrylate photopolymer configured for orthodontic indirect bonding tray fabrication on Carbon Digital Light Synthesis printers. The resin is supplied for use with a printer-specific, supplier-locked print profile rather than as a user-parameterized generic photopolymer. Methacrylate conversion proceeds by radical photopolymerization in the printer’s build zone, where an oxygen-permeable window creates a polymerization-inhibited layer at the interface; this oxygen-controlled dead zone permits continuous part growth while controlling the lower boundary of cure. The same oxygen sensitivity imposes strict handling limits: storage below the qualified temperature window elevates viscosity, and exposure of the open cassette to ambient ultraviolet or blue light can generate gel nuclei that subsequently appear as surface defects in the printed tray. Used within its intended indication, the resin produces a patient-specific transfer device for indirect orthodontic bracket bonding; it is not a direct restorative resin and is not qualified for long-term intraoral service.

    How Does an IBT-Grade Resin Differ from Printed Model and Splint Materials?

    Indirect bonding trays impose a different mechanical signature than printed dental models or occlusal splints. A model resin is optimized for dimensional stability during storage and for resistance to abrasion during stone or plaster handling; a splint resin is optimized for toughness and wear under occlusal load. An IBT methacrylate resin must preserve inter-bracket linear dimensions after post-cure while retaining enough strain tolerance to release over bonded brackets without fracture or permanent deformation. These requirements are not achieved by a single maximum modulus value; they are expressed in the relationship between flexural modulus, elongation at break, and water uptake, as measured under ISO 178:2019 or ISO 527-1:2019 conditions. Published data for this specific configuration is limited; direct substitution of a model resin therefore introduces unresolved risks in tray seating, because residual polymerization shrinkage and solvent swelling are not corrected by the IBT-specific workflow.

    The crosslink density of an IBT methacrylate is formulated within a narrower band than a model resin. Excessively high crosslink density creates a brittle tray that fractures at undercut withdrawal; insufficient crosslink density leaves residual unreacted methacrylate groups that can plasticize the matrix after cleaning. The resin therefore includes a tuned inhibitor package to extend bath life without suppressing surface cure. Because the working curve is lot-dependent, the user cannot infer processability from viscosity alone; penetration depth and critical dose must be contained within the supplier-defined window for the specific Carbon printer model. Compared with a printed model resin, the IBT formulation is not optimized for maximum surface hardness; compared with a splint resin, it is not formulated for prolonged cyclic occlusal loading.

    On a production Carbon M2 or M3 printer operating at laboratory ambient temperature, the cassette is installed and the material code is read by the machine; the validated IBT profile controls slice thickness, exposure dose, and build platform speed. Layer thickness is not user-editable within the locked clinical profile, because changing from the qualified slice increment alters the oxygen-inhibited layer balance and the resulting surface finish. In the continuous build zone, cure depth follows the Jacobs working curve, Cd = Dp ln(E0/Ec), where Dp is the penetration depth and Ec is the critical energy dose. A decrease in Ec from photoinitiator aging widens the working depth but may compromise adhesion to adjacent layers; an increase in Ec from inhibitor accumulation produces under-cured green parts and delamination in tray extensions.

    After printing, the green tray is transferred to the Carbon Smart Part Washer or an equivalent validated solvent unit. Residual resin film left on the tray retains methacrylate functionality and must be removed before post-cure; excessive solvent exposure, by contrast, swells the methacrylate network and lowers its glass transition temperature. The solvent selected for IBT processing is part of the locked workflow and should not be replaced with generic isopropanol unless the supplier has explicitly qualified that substitution. Incompletely dried thin sections are a known production failure mode on dental laboratory lines: solvent trapped in the tray body vaporizes during thermal post-cure and causes surface blistering or dimensional bowing. At ambient relative humidity above 60 %, extended drying is required before post-cure because absorbed water competes with methacrylate conversion and can produce surface tack.

    Post-cure is performed in a UV/visible chamber with a controlled dose; the post-cure recipe is time- and temperature-bounded because methacrylate conversion is exothermic. Thick tray sections retain heat, while thin bracket-transfer extensions dissipate heat rapidly; non-uniform curing therefore produces locked-in thermal gradients. The tray should be supported in the post-cure unit on a flat, non-reflective fixture to reduce free-state warpage. Published data for this specific configuration is limited; the supplier’s post-cure cycle must be treated as a critical process parameter rather than a default recommendation.

    Validated Printing Conditions and Bath Viscosity Control

    Viscosity is the dominant resin-side variable during serial production. Methacrylate viscosity falls with increasing temperature, but the printer’s optical path also heats the cassette during extended print runs. If the cassette begins a build at the low end of the qualified storage range, the dead zone thins and the build platform may pull vacuum against the window; if the cassette exceeds the upper end because of exothermic runoff, thermal polymerization in the bulk can produce microgel particles. Production experience on continuous DLS equipment shows that these particles appear as irregular surface defects, often concentrated at the trailing edge of drainage and on the first printed layers after idle periods. Operators should therefore record cassette temperature and reject builds that start outside the supplier-defined band. Manual dilution with reactive diluent is not permitted; dilution changes the critical energy dose and violates the serialized material traceability chain.

    Batch-to-batch variance is controlled through serialized cassetting, but the dental laboratory retains responsibility for verifying lot receipt conditions. A new resin lot should be qualified on a known reference geometry before full patient work begins. Because methacrylate initiators are sensitive to oxygen, opened cassettes have a finite use life; the supplier’s open-cassette use limit is a boundary condition, not a suggestion. If the resin shows a visible skin or an increase in viscosity after cold storage, the lot is rejected. The certificate of analysis lists lot-specific resin viscosity, photoinitiator absorbance, and cure depth; these are specification values, not general marketing descriptions.

    When Post-Cure Is Omitted or Truncated in the Dental Laboratory

    An under-post-cured IBT methacrylate tray retains a higher fraction of unreacted methacrylate groups. These residual groups can leach into the oral environment or react slowly under ambient light, causing progressive dimensional shift after the tray has been fitted. Clinically, this translates to bracket positions that drift between try-in and bonding. The failure is not always visible; a tack-free surface may exist over a core with incomplete network conversion. Therefore, post-cure cannot be shortened for production speed without a validated equivalence study. If the laboratory uses a broadband LED chamber instead of the supplier-recommended unit, the spectral overlap with the photoinitiator must be demonstrated. A chamber with high irradiance in the visible range but low emission at the required UV wavelength will fail to drive conversion, even if the displayed dose is high.

    Similarly, post-curing a tray still wet with cleaning solvent produces a plasticized matrix that may pass a flexural check but will creep under the seating force of bracket transfer. The supplier’s workflow sequences washing, drying, and post-cure as dependent operations; omitting the drying step invalidates the final part properties. The printed tray should not be allowed to rest in ambient sunlight before post-cure because uncontrolled photoinitiation can produce a hardened surface layer over a soft interior, a gradient failure that is difficult to detect prior to clinical use.

    Biocompatibility and Regulatory Verifications Are Required Before Clinical Use

    Patient contact is governed by the intended contact duration and tissue type. For an orthodontic transfer tray, the contact is transient but repeated across bonding visits; the laboratory or prescribing clinician must confirm that the supplier’s biological evaluation covers the intended use. The following matrix identifies verification points that are commonly required for a resin-based indirect bonding tray. The presence of a standard designation in a supplier file does not by itself establish compliance for a specific clinical workflow; the standard must be matched to the patient population and regulatory jurisdiction.

    Verification Area Standard or Regulatory Reference Required Evidence Point
    Biological evaluation planning ISO 10993-1:2018 Documented rationale for endpoints, contact duration, and material category
    Cytotoxicity ISO 10993-5:2009 Extract-based assay on fully post-cured printed specimens
    Irritation and delayed-type hypersensitivity ISO 10993-10:2010 Qualified sensitization and irritation data for cured resin
    Dental orthodontic base polymer requirements ISO 20795-2:2013 Mechanical, residual monomer, and water-related characteristics
    Quality management system ISO 13485:2016 Lot traceability, process validation, and post-market surveillance records
    European medical device regulatory framework Regulation (EU) 2017/745 Custom-made device documentation where applicable to the patient-specific tray
    Chemical safety in the European Union EC 1907/2006 REACH registration and safety data sheet compliance for methacrylate components
    Restriction of hazardous substances Directive 2011/65/EU RoHS conformity declaration where required for electronic manufacturing inputs

    Incompatibilities with solvent substitution and third-party additives are the principal operational boundaries. The resin should not be mixed with amine-based accelerators, because tertiary amines can form redox initiation systems with methacrylate peroxides and trigger exothermic polymerization in the cassette. Contact with metal naphthenates or copper-containing alloys should also be avoided before cure, because these species can alter radical kinetics. The printed tray is intended for short-term use as an indirect bonding transfer device; repeated autoclaving or chemical disinfection is not a qualified reprocessing route. Once the tray has transferred brackets, it should be discarded as medical waste according to local regulations. No additional clinical applications are claimed beyond the patient-specific indirect bonding workflow.

    ТОП